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FAQ

Frequently asked questions on W&H products and helpful descriptions on the topic of cleaning and care.

Surgical Devices

Straight & Contra-angle Handpieces

Couplings

Accessories

Saw Handpieces

Turbines

Implant stability measurement

  • Osstell Classic (3)
    • How does the measurement of the ISQ work?
      > To measure the ISQ of an implant, you first screw a so called SmartPeg into the placed implant. The SmartPeg, with its magnet on top, works like a small tuning fork. The magnet on the SmartPeg is ‘hit’ with magnetic pulses, from the probe, which makes the SmartPeg vibrate. Due to the stiffness in the interface between the implant surface and the bone the SmartPeg will vibrate accordingly. The more dense the bone is the higher stability and the higher ISQ value.
      isq scale
    • Where can I buy the SmartPegs?
      Please contact your local W&H partner
      The sale of SmartPegs will be defined per country
      The surgeon will receive 5 free SmartPegs. A voucher will be provided with the delivery of the product.
    • What does ISQ stand for?
      The abbreviation ISQ stands for Implant Stability Quotient. It is a value between 1 and 100 and gives the surgeon an insight of the implant stability after placing the implant. With the ISQ value the surgeon can monitor the osseointegration.
  • Osstell Beacon (4)
    • Is the ISQ scientifically proven?
      The Osstell ISQ technology is proven by over 1400 scientific studies. These studies have shown, that torque and ISQ correlate.
    • How does the measurement of the ISQ work?
      > To measure the ISQ of an implant, you first screw a so called SmartPeg into the placed implant. The SmartPeg, with its magnet on top, works like a small tuning fork. The magnet on the SmartPeg is ‘hit’ with magnetic pulses, from the probe, which makes the SmartPeg vibrate. Due to the stiffness in the interface between the implant surface and the bone the SmartPeg will vibrate accordingly. The more dense the bone is the higher stability and the higher ISQ value.
      isq scale
    • Where can I buy the SmartPegs?
      Please contact your local W&H partner
      The sale of SmartPegs will be defined per country
      The surgeon will receive 5 free SmartPegs. A voucher will be provided with the delivery of the product.
    • What does ISQ stand for?
      The abbreviation ISQ stands for Implant Stability Quotient. It is a value between 1 and 100 and gives the surgeon an insight of the implant stability after placing the implant. With the ISQ value the surgeon can monitor the osseointegration.

Accessories

  • W&H Osstell ISQ module (6)
    • Is the ISQ scientifically proven?
      The Osstell ISQ technology is proven by over 1400 scientific studies. These studies have shown, that torque and ISQ correlate.
    • What’s the difference between torque and ISQ?
      Torque is a one time, static measurement at the time of placement of the implant and cannot be repeated later on in a non-invasive way. Osstell ISQ measures the lateral stability of the implant and the measurements can be repeated in a non-invasive, dynamic way to monitor the development of osseointegration.
    • Is every new Implantmed compatible with the W&H Osstell ISQ module?
      Yes. All control units SI-1023, SI-1015 and SI-1010 can be upgraded with the W&H Osstell ISQ module
    • How does the measurement of the ISQ work?
      > To measure the ISQ of an implant, you first screw a so called SmartPeg into the placed implant. The SmartPeg, with its magnet on top, works like a small tuning fork. The magnet on the SmartPeg is ‘hit’ with magnetic pulses, from the probe, which makes the SmartPeg vibrate. Due to the stiffness in the interface between the implant surface and the bone the SmartPeg will vibrate accordingly. The more dense the bone is the higher stability and the higher ISQ value.
      isq scale
    • Where can I buy the SmartPegs?
      Please contact your local W&H partner
      The sale of SmartPegs will be defined per country
      The surgeon will receive 5 free SmartPegs. A voucher will be provided with the delivery of the product.
    • What does ISQ stand for?
      The abbreviation ISQ stands for Implant Stability Quotient. It is a value between 1 and 100 and gives the surgeon an insight of the implant stability after placing the implant. With the ISQ value the surgeon can monitor the osseointegration.
  • SmartPeg (20)
    • How many times can the SmartPeg be used?
      The reusable SmartPeg can be used for up to 20 reprocessing cycles, as long as its integrity and performance are maintained. If inspection reveals wear, deformation, corrosion, damaged threads, or any loss of functional compatibility, the SmartPeg must be discarded, even if it has been processed fewer than 20 times. The single-use SmartPeg is intended for one treatment session only and must not be reprocessed.
    • Can I combine single-use and reusable SmartPegs in the same treatment session?
      Yes. You can combine single-use and reusable SmartPegs in the same treatment session. The only requirement is that you use the correct SmartPeg type number for the specific implant or abutment you are measuring. Whether the SmartPeg is intended for single-use or reuse does not affect the measurement.
    • Why can the reusable SmartPeg be cleaned and sterilized, but the single-use SmartPeg cannot, even though both are made of aluminium?
      The reusable SmartPeg features a special protective surface coating – one on the SmartPeg body and another black protective coating on the magnet. These coatings provide resistance to moisture, cleaning agents, wear, and corrosion, ensuring that the SmartPeg maintains its performance throughout the validated number of reprocessing cycles.
    • Does a reusable SmartPeg provide the same ISQ values as a single use SmartPeg?
      Yes. Osstell is also the only company offering both a sterile single-use and a reusable SmartPeg made of aluminium, supported by more than 1,500 published studies on the ISQ method. With the Osstell original ISQ scale and SmartPegs, no conversion tables or correction factors are needed. The measured ISQ value is the true value, regardless of whether you use a single-use or a reusable SmartPeg.
    • Is there a visual difference between the single-use and reusable SmartPeg?
      Yes. The reusable and single use SmartPegs are designed to be easily distinguishable: • The single-use SmartPeg is supplied sterile, has an aluminium coloured (non contrasting) magnet, and does not have any laser marked identifiers. • The reusable SmartPeg has a black magnet on top and carries laser marked type and LOT numbers for identification and traceability.
    • How are the different SmartPegs packed?
      SmartPegs are available in different packaging formats depending on whether they are single-use or reusable:
      Single-use SmartPegs
      • Delivered sterile.
      • Supplied in packs of 5 pieces, in a single sterile barrier system with protective outer packaging.
      • Intended for one treatment session only and must not be reused.

      Reusable SmartPegs
      • Delivered non-sterile in individual packaging.
      • Must be cleaned, disinfected and sterilized before the first clinical use and after each subsequent use (see IFU).
    • Are there any studies that prove the Osstell method?
      There are currently thousands of scientific publications in which Osstell has been used as part of the study protocol. These abstracts can be explored through our searchable database under Osstell.com/scientific-database. In all these studies, Osstell SmartPegs – made of aluminium – have been used, providing the consistent and validated measurement standard upon which the ISQ evidence base is built.
    • Does the way the SmartPeg is tightened affect the ISQ value?
      Yes. The ISQ value can be affected if the SmartPeg is not mounted correctly. For accurate measurements, the SmartPeg should be finger-tightened using the SmartPeg Mount (approximately 4–6 Ncm). At this thightening torque, the SmartPeg has firm, stable contact with the implant, and the resulting ISQ value is consistent – typically within ±2 ISQ units. If the SmartPeg is not fully mounted:
      • The contact becomes unstable, and the ISQ value may appear falsely low.
      If too much force is applied:
      • Overtightening does not improve accuracy. It may damage the SmartPeg threads.
      - A reusable SmartPeg may be damaged so it cannot be used again.
      - A single-use or reusable SmartPeg may have its threads deformed, leading to inaccurate measurements during a session or, in the worst case, a broken SmartPeg.
    • How should I mount the SmartPeg to the implant?
      Whether you are using a single-use or reusable SmartPeg, it should always be mounted using the SmartPeg Mount and tightened to a torque of approximately 4–6 Ncm, which is usually described as finger-tight. This ensures that the SmartPeg is correctly positioned and accurate ISQ measurements without risking damage to the implant connection or SmartPeg.
    • Do I need a torque tool to tighten the SmartPeg correctly?
      No. A torque wrench must not be used to tighten the SmartPeg. SmartPegs should always be mounted using the SmartPeg Mount and tightened to a torque of approximately 4–6 Ncm, which is usually described as finger-tight. This ensures that the SmartPeg is correctly positioned without risking damage to the implant connection.
    • How should the reusable SmartPeg and the SmartPeg Mount be cleaned and sterilized?
      Prior to the first clinical use, and after each use the reusable products must be cleaned, disinfected and sterilized according to the instructions in the quickguide that is found here: here
    • Does using the Osstell measuring device affect the implant?
      No. The Osstell measurement does not affect the implant. The measuring device only makes the SmartPeg vibrate. The SmartPeg’s magnet is activated by very low magnetic pulses generated by the device. The technique is objective, gentle, and highly reproducible.
    • How do I select the correct SmartPeg for my implant?
      Different implants require specific SmartPegs to ensure accurate measurement. Each SmartPeg is matched to a particular implant system and connection type. You can find the correct SmartPeg for your implant in the SmartPeg Reference Guide – click here to access it.
    • Which Osstell products can be autoclaved?
      The following products can be autoclaved (over-pressurized steam up to 135°C):
      – SmartPeg Mount
      – Reusable SmartPeg
      – Probe (IDx)
      Please note that single-use SmartPegs are disposable and cannot be autoclaved!
    • How does the Osstell technology work?
      Osstell measures implant stability using Resonance Frequency Analysis (RFA). The small SmartPeg, that you attach to the implant is equipped with a tiny magnet on top. When the probe sends magnetic pulses, the SmartPeg starts to vibrate – similar to a very small tuning fork.
      How it works:
      1. The probe sends magnetic pulses.
      These pulses make the SmartPeg vibrate without physical contact.
      2. The vibration intensity changes depending on how stable the implant is.
      • A stable implant (good bone support) makes the SmartPeg vibrate faster.
      • A less stable implant makes it vibrate slower.
      3. The device converts this vibration into an ISQ value
      Higher stability → higher frequency → higher ISQ value
      Lower stability → lower frequency → lower ISQ vaue
      The measurement takes less than a second, and the ISQ value is displayed immediately.
    • Why do I get unexpected values or no measurements at all?
      Several factors may lead to unexpected ISQ values or failure to obtain a reading:
      1. Incorrect use or condition of the SmartPeg
      • Single-use SmartPegs: These are intended for one treatment session and one patient only. Reusing a single use SmartPeg may lead to worn threads and unreliable measurements.
      • Reusable SmartPegs: Ensue properly cleaning, inspection, and that they are not damaged. Wear, deformation or contamination can affect performance.
      2. Wrong SmartPeg type selected
      Make sure you have selected the correct SmartPeg for the specific implant system and connection. See SmartPeg Reference Guide: osstell.com/smartpegguide 3. Tissue or debris in the implant connection
      Bone fragments, soft tissue or fluid between the implant interface and the SmartPeg can prevent proper seating. Clean the implant prosthetic connection thoroughly before attaching the SmartPeg.
      4. Electromagnetic interference Nearby sources of electromagnetic disturbance may disrupt the measurement. If possible, remove or switch off the source of interference.
      5. Incorrect probe positioning Hold the instrument tip 2–4 mm away from the SmartPeg and align it correctly towards the top of the peg. Do not touch the magnet.
    • What should I do if no ISQ value is displayed?
      If no ISQ value is displayed, it usually means the SmartPeg’s vibration is not being clearly detected by the measuring device. Several factors can cause this, and most of which are easy to resolve:
      1. Distance to measuring device is too great
      The measuring device should normally be held 2–4 mm away from the magnet on the top of the SmartPeg. Do not touch the magnet.
      If no value is displayed, move the measuring device closer to the magnet until a signal is detected.
      2. Angle needs adjustment
      The magnetic field is directional, so the orientation of the measuring device is important. Measurements should be taken at an angle of approximately 45 degrees to the top of the SmartPeg.
      3. Ensure you are using the correct SmartPeg type for the specific implant
      Use this link to find the correct SmartPeg type: Find my SmartPeg.
      4. Soft tissue damping
      Surrounding tissue can sometimes dampen the vibration more than expected. Holding the measuring device a bit closer usually compensates for this.
      5. The implant platform is not clean Ensure the implant platform is clean and free of debris, so the SmartPeg seats properly and transmits its vibration.
      6. The SmartPeg is worn or damaged
      • If you are using a reusable SmartPeg, inspected it before use.
      A reusable SmartPeg that is worn out, bent, or has damaged threads may not vibrate correctly – and the measuring device may not be able to acquire any readings.
      • A single‑use SmartPeg is intended for use in one treatment session only.
      • Ensure the SmartPeg is properly seated on the implant and that it is not in contact with the surrounding tissue, as this can prevent accurate signal detection and may result in no or an incorrect ISQ value.
      7. Electromagnetic interference
      Strong electromagnetic interference sources nearby may disturb the measurement. (See the FAQ on “Electromagnetic noise” for details.)
    • How do I measure and record ISQ at an abutment?
      You can measure and record ISQ at abutment level in OsstellConnect. However, it is important to follow the correct clinical measurement procedure to obtain accurate values.
      How to measure ISQ at abutment level:
      1. Perform an implant level measurement first, before placing the abutment.
      2. Measure again at abutment level during the same session, using a SmartPeg made for abutment level measuring.
      3. Determine the offset by noting the difference between implant level and abutment level ISQ. This offset remains stable throughout the healing phase and should be considered when interpreting follow-up measurements.
      4. At all subsequent appointments, measure on the abutment and apply the same offset to determine the true implant ISQ.

      How to record the measurement in OsstellConnect:
      1. Access patient record, select the patient and the implant in the tooth chart. Click ‘Add abutment’, select the abutment, and save the data.
      2. Select ‘Measure stability’ and choose ‘Abutment’, under Measurement level. Measure on the abutment as you would at implant level, and save.
      3. To check the stability progression, open the Stability tab and toggle ‘Show abutment’. You can also enable ‘Show details’ to view buccal–lingual and mesial–distal ISQ values. For a more detailed explanation and clinical guidance, see our blog post here
    • Why do I have to take two measurements at the same occasion?
      ISQ should always be measured in two directions, as implant stability can vary depending on the amount of surrounding bone. Measuring from two angles ensures that both the most and the least stable directions are captured. To do this, take one measurement in the buccal-lingual direction and one in the mesial-distal direction. These two ISQ values represent the different stability directions. Sometimes the values are identical; sometimes they differ. If the two measurements differ, always rely on the lowest ISQ value, as it reflects the weakest direction and therefore provides the most clinically relevant information about implant stability.
    • Why is the Osstell ISQ scale important?
      The Osstell ISQ scale is important because it provides precise insights into the progress of osseointegration, helping clinicians determine the optimal timing for prosthetic loading and ensuring a safe surgical protocol.
  • Piezomed Instruments (5)
    • How are the instruments prepared for cleaning?
      a. Preparation in the ultrasonic bath:
      - Place the instruments in the instrument tray and lower into the ultrasonic bath.
      - Use cleaning agents and disinfectants suitable for hand instruments (probes, mirrors, forceps, etc.).
      DO NOT USE a bur bath, as this is very aggressive.
      - After cleaning in the ultrasonic bath, rinse adequately with water to remove any remnants of the cleaning agent and disinfectant from the coolant channels.
      - Blow dry with compressed air after rinsing
      - Replace dried instruments in the instrument tray and package for sterilization

      b. Mechanical preparation in the cleaning unit and disinfector
      - Use the cleaning adapter for cleaning units and disinfectors (see Instructions for Use – Accessories)
      - After preparation in the cleaning unit and disinfector, check that the coolant channels are dry and, if necessary, dry again with compressed air.
    • Can third-party instruments be used on the Piezomed?
      No
      a. Different thread
      b. The Piezomed instrument detection cannot detect third-party instruments
    • Can Piezomed instruments also be used on third-party devices?
      No
      a. Different thread
      b. Third-party devices are not engineered for the correct resonance point – instrument fails to oscillate.
    • How long do the instruments last and when should they be replaced?
      The useful service life of the instruments is determined by the length of time they are used - reprocessing and sterilization cycles only have a marginal influence on the live span.
      a. Instruments need to be replaced
      - If there is a loss of cutting power while working
      - In case of visible damage on the cutting portion or the shank of the instrument.
      b. Saws must be replaced if
      - Teeth are broken off
      - Teeth are worn and cutting power drops
      - In case of visible damage on the cutting portion or the shank of the instrument.
      c. Diamond-coated instruments must be replaced
      - As soon as the diamond coating is worn
      - In case of visible damage on the cutting portion or the shank of the instrument.
      - For USA only - Diamond-coated instruments are considered single-use by the FDA.
    • Is it necessary for the torque driver to engage audibly when tightening the instrument?
      Yes, it must engage audibly once, as otherwise the required torque is not achieved.

Electric Motor

Reprocessing Devices

  • Assistina TWIN (7)
    • Why is there no rotational lubrication option in the Assistina TWIN?
      The oil is atomized in the Assistina TWIN before it is enters the instrument. This ensures full coverage of the gear parts, eliminating the need for technically complex and time-consuming rotational lubrication. However, there is no negative impact on the maintenance quality: the results of a maintenance operation correspond to those achieved with the Assistina 301 Plus.
    • What instrument adaptors are available for the Assistina TWIN?
      All adaptors that are suitable for the Assistina 3x2/3x3 can also be used in the Assistina TWIN. There is only one exception: the RM/ISO adaptor for the Assistina 3x2/3x3 is not compatible with the Assistina TWIN. Quick Connect adaptors ISO and RM can be used for the Assistina TWIN instead. An overview of all adaptors is available on the product website.
    • Why does the Assistina TWIN have a HEPA filter?
      During the maintenance process in the Assistina TWIN, the rotating parts are lubricated with oil and the spray channels rinsed with cleaning solution. These liquids are introduced to the handpieces using compressed air, which produces aerosols that may contain potentially contaminated body fluids (e.g. blood and saliva). In order to ensure that the apparatus poses no risk to the user, the patient or third parties, the law stipulates that aerosols must be prevented from leaking out of the apparatus. We make sure of this by using active suction and the HEPA filter. This HEPA filter must of course be changed regularly, which is why the lifespan of the filter is matched exactly to the capacity of the two cartridges. The HEPA filter therefore reaches the end of its service life once one set of cartridges has been used.
    • Which processing steps are carried out in the Assistina TWIN?
      • Cleaning the spray channels with W&H Activefluid
      • Lubricating the rotating parts with W&H Service Oil
      • Throughout the maintenance process, potentially contaminated aerosols are extracted from the process chamber and the exhaust air is cleaned using a HEPA filter.
    • How does the user know when the TWIN Care Set needs to be replaced?
      The intelligent process monitoring system documents the number of maintenance cycles that have been performed, thereby automatically calculating the number of instruments that can be serviced with the remaining quantity of fluid. The user receives an alert 300 cycles before the cartridge needs replacing (the oil and cleaner LEDs on the top of the unit turn yellow in colour).
    • How often does the TWIN Care Set need to be replaced?
      The consumption volumes for each instrument are 0.07 ml of oil and 0.07 ml of cleaning solution. This gives a maximum capacity of 2857 cycles. In reality, the value is around 2800 to 2850 cycles, as initial filling is also required and the fill quantity of the cartridges is subject to certain tolerances that are regulated by the applicable standards.
    • What does HEPA mean, and what is filtered out of the air?
      HEPA is short for 'High Efficiency Particular Air', and the filter is classified as HEPA class E11. This means that the filter retains all particles larger than 1 µm, which includes, among other things, a wide range of bacteria and viruses, suspended particles such as dust and respirable aerosols.
  • Assistina ONE (8)
    • What does HEPA mean, and what is filtered out of the air?
      HEPA is short for 'High Efficiency Particular Air', and the filter is classified as HEPA class E11. This means that the filter retains all particles larger than 1 µm, which includes, among other things, a wide range of bacteria and viruses, suspended particles such as dust and respirable aerosols.
    • Why there is no rotational lubrication option in the Assistina One?
      The oil is atomized in the Assistina One before it enters the instrument. This ensures full coverage of the gear parts, eliminating the need for technically complex and time-consuming rotational lubrication. However, there is no negative impact on the maintenance quality.
    • What is the difference between oil nebulization and rotational lubrication?
      Final result is the same, but in a shorter time. In the nebulization system, oil is nebulized in the adaptor before it is blown into the handpiece. An oil mist coats all gear parts.
    • What instrument adaptors are available for the Assistina One?
      All adaptors that are suitable for the Assistina 3x2/3x3 can also be used in the Assistina One. There is only one exception: the RM/ISO adaptor for the Assistina 3x2/3x3 is not compatible with the Assistina One. Quick Connect adaptors ISO and RM can be used for the Assistina One instead. An overview of all adaptors is available in the product website.
    • Why does the Assistina One have a HEPA filter?
      During the maintenance process in the Assistina One, the rotating parts are lubricated with oil, and the spray channels rinsed with cleaning solution. These liquids are introduced to the handpieces using compressed air, which produces aerosols that may contain potentially contaminated body fluids (e.g. blood and saliva). In order to ensure that the apparatus poses no risk to the user, the patient or third parties, the legislation stipulates that aerosols must be prevented from leaking out of the apparatus. We make sure of this by using active suction and the HEPA filter. This HEPA filter must of course be changed regularly, which is why the lifespan of the filter is matched exactly to the capacity of the two cartridges. The HEPA filter therefore reaches the end of its service life once one set of cartridges has been used.
    • How does the user know when the ONE Care Set needs to be replaced?
      The ONE Care Set must be replaced when the cartridges are empty. The levels can be checked thanks to the device's fill level indicators, located on the right and left sides.
    • How often does the ONE Care Set needs to be replaced?
      The consumption volumes for each instrument are 0.07 ml of oil and 0.07 ml of cleaning solution. This gives a maximum capacity of 2857 cycles. The value is around 2800 to 2850 cycles, as initial filling is also required and the fill quantity of the cartridges is subject to certain tolerances that are regulated by the applicable standards.
    • How do you replace the ONE Care Set?
      The two cartridges and the filter can be changed easily without any tools. The fluid is supplied via tapping needles in the bottom of the cartridge spaces that penetrate the cartridge membrane, thereby drawing the fluid out of the cartridge. The two cartridges have different shapes to ensure that the two fluid types cannot be mixed up. In addition, it is only possible to install the HEPA filter incorrectly by using force, which is not necessary.

Cordless Devices

Air polisher

Straight & Contra-angle Handpieces

Accessories

Water Treatment Devices

  • Osmo (1)
    • Which water quality should I use for my Lexa Plus sterilizer?
      The water quality for sterilizers is internationally specified by standards and directives. The reasons for this are that your sterilizer can be seriously damaged by it or the sterilization can be jeopardised. Consequently, only water with conductivity of less than 10 µS/cm in North America and 15 µS/cm for the rest of the world should be used for your W&H sterilizer. The Multidem system and OSMO are especially designed to prepare suitable water (see chapter “Water quality” in the Instructions for Use).

Straight & Contra-angle Handpieces

Piezo Scaler

Sterilizers

  • MS Sterilizer (2)
    • What is validation?
      Validation is a testing procedure carried out by an official authority, proving the effectiveness of your sterilizer. Compulsories and frequency of validation are regulated by local/national guidelines.
    • Do I need to document the results of all periodic tests?
      W&H recommends recording all periodic tests, repairs and modifications on the sterilizer in a logbook including date and signature of the person who carried out the test or other activity. Compulsoriness of recording is regulated by local/national guidelines.
  • Lara (24)
    • What is validation?
      Validation is a testing procedure carried out by an official authority, proving the effectiveness of your sterilizer. Compulsories and frequency of validation are regulated by local/national guidelines.
    • Do I need to document the results of all periodic tests?
      W&H recommends recording all periodic tests, repairs and modifications on the sterilizer in a logbook including date and signature of the person who carried out the test or other activity. Compulsoriness of recording is regulated by local/national guidelines.
    • How long should I archive the documentation of regular tests?
      Keep the results according to your country/regional specific laws and guidelines. Those records can be of assistance in case of service as well.
    • Does my sterilizer need any periodic qualification/validation?
      Validation generally comprises a range of tests defined in internationally recognised standards. These tests begin for every device with the factory tests at W&H. In addition, corresponding documentation is included with your device. Prior to commissioning the device at your premises, the technician performs further checks to ensure the device functions correctly. Then, depending on the national/regional laws and directives, the device must be subjected to a so-called renewed performance qualification at regular intervals. For further information, please contact your dealer.
    • Whom should I contact to validate and maintain my sterilizer?
      Validation shall be carried out by an official authority. Maintenance tasks shall be carried out by a qualified and authorized technician.
    • How do I change consumable components on my sterilizer?
      Consumable replacement instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu; • in the Consumables & Accessories and Video Tutorial section of this web site.
    • How do I clean the water tanks and what products should I use?
      Water tank cleaning instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu;
      • in the Consumables & Accessories and Video Tutorial section of this web site.
    • Should I pouch wrap my instruments and how long can I store them after sterilization?
      To ensure that your instruments are stored in a sterile state from their successful sterilization until they are used, W&H recommends wrapping them in suitable sterile barrier systems before sterilization. The recommended storage period can be found in the recommendations of the wrapping material manufacturer. For further information, please contact your dealer.
    • The sterilizer remains switched OFF.
      POSSIBLE CAUSE
      The main switch or network circuit breaker is OFF.
      SOLUTION
      Activate the main switch or network circuit breaker (ON).

      POSSIBLE CAUSE
      No voltage at the socket.
      SOLUTION
      Check the building electrical supply.

      POSSIBLE CAUSE
      The power cord is not connected properly
      SOLUTION
      Check and connect the power cord properly
    • Water is leaking at the front of the sterilizer.
      POSSIBLE CAUSE
      Leaks through the chamber door seal.
      SOLUTION
      Clean or replace the door seal. Clean the door surface facing the chamber.

      POSSIBLE CAUSE
      Internal leak.
      SOLUTIONS
      Contact an authorized W&H service partner.
    • At the end of the cycle, there is residual water in the chamber
      POSSIBLE CAUSE
      Sterilizer not properly levelled
      SOLUTION
      Place the sterilizer on a flat, levelled surface.

      POSSIBLE CAUSE
      Overloaded chamber
      SOLUTION
      Comply with the maximum load weight limits for each type of load. Always use the chamber rack for trays and cassettes.

      POSSIBLE CAUSE
      Chamber filter clogged
      SOLUTION
      Remove and clean the chamber filter.

      POSSIBLE CAUSE
      Load incorrectly placed
      SOLUTION
      Follow the recommendations as listed in chapter “Load maintenance and preparation” in the Instructions for Use.
    • The sterilizer enters into “Standby mode” immediately after being switched on.
      POSSIBLE CAUSE
      The unit was turned off while in standby mode.
      SOLUTION
      Press the “Standby mode” button to exit.
    • When starting a cycle, the chamber door locks but re-opens immediately. The “Open the door” message appears.
      POSSIBLE CAUSE
      Door seal not properly placed.
      SOLUTION
      Ensure that the door seal is correctly inserted around the whole circumference.

      POSSIBLE CAUSE
      Door jammed by external objects or by the load itself
      SOLUTION
      Remove any objects interfering with the chamber door. Check for interference between the door and the chamber furniture and/or the load.
    • Stains, spots or colour change on instruments.
      POSSIBLE CAUSE
      Instruments rinsed with tap water and not dried before sterilization.
      SOLUTION
      Ensure that instruments are rinsed with distilled or demineralized water and completely dry before they are placed in the sterilizer.

      POSSIBLE CAUSE
      Use of water of poor quality or water containing chemical substances
      SOLUTION
      Drain both water tanks. Use good quality water (see chapter “Water quality” in the Instructions for Use).

      POSSIBLE CAUSE
      Organic or chemical residues on the instruments
      SOLUTION
      Clean, rinse and dry instruments before placing them in the sterilizer (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Dirt in chamber, trays, tray rack.
      SOLUTION
      Clean the chamber and wash the chamber furniture

      POSSIBLE CAUSE
      Contact between instruments of different materials
      SOLUTION
      Ensure that instruments of different materials do not touch each other (aluminum, carbon or stainless steel, etc.); place them on different trays or cassettes or pouch them (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Scale deposits on the chamber
      SOLUTION
      Clean the chamber and use good quality water (see chapter “Water quality” in the Instructions for Use).
    • No cycles are stored in the cycle history menu
      POSSIBLE CAUSE
      An electronic board was replaced when serviced.
      SOLUTION
      The memory of the old board cannot be restored. Consult the cycle history in the USB pen drive.
    • Warning about saving to the USB (HTML and SCL files)
      POSSIBLE CAUSE
      The USB pen drive is disconnected or full.
      SOLUTION
      Check presence and condition of the USB pen drive. If the problem persist, contact an authorized W&H service partner.
    • Warning about programmed maintenance.
      POSSIBLE CAUSE
      The maintenance program needs to be carried out.
      SOLUTION
      Contact an authorized W&H service partner.
    • The cycle report printer does not work.
      POSSIBLE CAUSE
      Printer not properly connected or not powered
      SOLUTION
      Check the data and the power connection to the printer.
    • The sterilizer is connected to an automated water supply system, there is no clean water in the tank and the automatic water filling does not fill the water.
      POSSIBLE CAUSE
      Water filling system not connected.
      SOLUTION
      Connect the water filling system to the sterilizer. (see Instructions For Use).

      POSSIBLE CAUSE
      When the water filling system attempted to fill the tank, water was temporarily unavailable.
      SOLUTION
      Since the water tank filling is attempted only once in-between cycle execution, this event inhibits water feeding. Switch the sterilizer OFF and then ON again.
      Check the external water supply system.
      Check for water leaks from the sterilizer.

      POSSIBLE CAUSE
      Faulty MIN water level sensor in the clean water tank
      SOLUTION
      Contact an authorized W&H service partner.
    • The sterilization (PROCESS) phase of a sterilization cycle was longer than expected.
      POSSIBLE CAUSE
      The chamber temperature dropped below the minimum threshold and the software performed a successful recovery
      SOLUTION
      Wait for cycle completion. If the problem occurs frequently, contact an authorized W&H service partner.
    • Warning about consumable replacement.
      POSSIBLE CAUSE
      A consumable needs to be replaced.
      SOLUTION
      Order the requested consumable (door seal and HEPA/bacteriological filter) and replace it. See the chapter “Maintenance” in the Instructions for Use.
    • What is the maximum noise level of the Lexa Plus sterilizer?
      The max. noise level of the Lexa Plus is 70 dB.
    • Which water quality should I use for my Lexa Plus sterilizer?
      The water quality for sterilizers is internationally specified by standards and directives. The reasons for this are that your sterilizer can be seriously damaged by it or the sterilization can be jeopardised. Consequently, only water with conductivity of less than 10 µS/cm in North America and 15 µS/cm for the rest of the world should be used for your W&H sterilizer. The Multidem system and OSMO are especially designed to prepare suitable water (see chapter “Water quality” in the Instructions for Use).
    • Do I need to carry out periodic testing on my W&H Sterilizer?
      All W&H sterilizers features test cycles (B&D/Helix test, Vacuum test). Compulsory and frequency of testing are regulated by local/national guidelines.
  • Lina (24)
    • What is validation?
      Validation is a testing procedure carried out by an official authority, proving the effectiveness of your sterilizer. Compulsories and frequency of validation are regulated by local/national guidelines.
    • Do I need to document the results of all periodic tests?
      W&H recommends recording all periodic tests, repairs and modifications on the sterilizer in a logbook including date and signature of the person who carried out the test or other activity. Compulsoriness of recording is regulated by local/national guidelines.
    • How long should I archive the documentation of regular tests?
      Keep the results according to your country/regional specific laws and guidelines. Those records can be of assistance in case of service as well.
    • Does my sterilizer need any periodic qualification/validation?
      Validation generally comprises a range of tests defined in internationally recognised standards. These tests begin for every device with the factory tests at W&H. In addition, corresponding documentation is included with your device. Prior to commissioning the device at your premises, the technician performs further checks to ensure the device functions correctly. Then, depending on the national/regional laws and directives, the device must be subjected to a so-called renewed performance qualification at regular intervals. For further information, please contact your dealer.
    • Whom should I contact to validate and maintain my sterilizer?
      Validation shall be carried out by an official authority. Maintenance tasks shall be carried out by a qualified and authorized technician.
    • How do I change consumable components on my sterilizer?
      Consumable replacement instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu; • in the Consumables & Accessories and Video Tutorial section of this web site.
    • How do I clean the water tanks and what products should I use?
      Water tank cleaning instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu;
      • in the Consumables & Accessories and Video Tutorial section of this web site.
    • Should I pouch wrap my instruments and how long can I store them after sterilization?
      To ensure that your instruments are stored in a sterile state from their successful sterilization until they are used, W&H recommends wrapping them in suitable sterile barrier systems before sterilization. The recommended storage period can be found in the recommendations of the wrapping material manufacturer. For further information, please contact your dealer.
    • The sterilizer remains switched OFF.
      POSSIBLE CAUSE
      The main switch or network circuit breaker is OFF.
      SOLUTION
      Activate the main switch or network circuit breaker (ON).

      POSSIBLE CAUSE
      No voltage at the socket.
      SOLUTION
      Check the building electrical supply.

      POSSIBLE CAUSE
      The power cord is not connected properly
      SOLUTION
      Check and connect the power cord properly
    • Water is leaking at the front of the sterilizer.
      POSSIBLE CAUSE
      Leaks through the chamber door seal.
      SOLUTION
      Clean or replace the door seal. Clean the door surface facing the chamber.

      POSSIBLE CAUSE
      Internal leak.
      SOLUTIONS
      Contact an authorized W&H service partner.
    • At the end of the cycle, there is residual water in the chamber
      POSSIBLE CAUSE
      Sterilizer not properly levelled
      SOLUTION
      Place the sterilizer on a flat, levelled surface.

      POSSIBLE CAUSE
      Overloaded chamber
      SOLUTION
      Comply with the maximum load weight limits for each type of load. Always use the chamber rack for trays and cassettes.

      POSSIBLE CAUSE
      Chamber filter clogged
      SOLUTION
      Remove and clean the chamber filter.

      POSSIBLE CAUSE
      Load incorrectly placed
      SOLUTION
      Follow the recommendations as listed in chapter “Load maintenance and preparation” in the Instructions for Use.
    • The sterilizer enters into “Standby mode” immediately after being switched on.
      POSSIBLE CAUSE
      The unit was turned off while in standby mode.
      SOLUTION
      Press the “Standby mode” button to exit.
    • When starting a cycle, the chamber door locks but re-opens immediately. The “Open the door” message appears.
      POSSIBLE CAUSE
      Door seal not properly placed.
      SOLUTION
      Ensure that the door seal is correctly inserted around the whole circumference.

      POSSIBLE CAUSE
      Door jammed by external objects or by the load itself
      SOLUTION
      Remove any objects interfering with the chamber door. Check for interference between the door and the chamber furniture and/or the load.
    • Stains, spots or colour change on instruments.
      POSSIBLE CAUSE
      Instruments rinsed with tap water and not dried before sterilization.
      SOLUTION
      Ensure that instruments are rinsed with distilled or demineralized water and completely dry before they are placed in the sterilizer.

      POSSIBLE CAUSE
      Use of water of poor quality or water containing chemical substances
      SOLUTION
      Drain both water tanks. Use good quality water (see chapter “Water quality” in the Instructions for Use).

      POSSIBLE CAUSE
      Organic or chemical residues on the instruments
      SOLUTION
      Clean, rinse and dry instruments before placing them in the sterilizer (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Dirt in chamber, trays, tray rack.
      SOLUTION
      Clean the chamber and wash the chamber furniture

      POSSIBLE CAUSE
      Contact between instruments of different materials
      SOLUTION
      Ensure that instruments of different materials do not touch each other (aluminum, carbon or stainless steel, etc.); place them on different trays or cassettes or pouch them (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Scale deposits on the chamber
      SOLUTION
      Clean the chamber and use good quality water (see chapter “Water quality” in the Instructions for Use).
    • No cycles are stored in the cycle history menu
      POSSIBLE CAUSE
      An electronic board was replaced when serviced.
      SOLUTION
      The memory of the old board cannot be restored. Consult the cycle history in the USB pen drive.
    • Warning about saving to the USB (HTML and SCL files)
      POSSIBLE CAUSE
      The USB pen drive is disconnected or full.
      SOLUTION
      Check presence and condition of the USB pen drive. If the problem persist, contact an authorized W&H service partner.
    • Warning about programmed maintenance.
      POSSIBLE CAUSE
      The maintenance program needs to be carried out.
      SOLUTION
      Contact an authorized W&H service partner.
    • The cycle report printer does not work.
      POSSIBLE CAUSE
      Printer not properly connected or not powered
      SOLUTION
      Check the data and the power connection to the printer.
    • The sterilizer is connected to an automated water supply system, there is no clean water in the tank and the automatic water filling does not fill the water.
      POSSIBLE CAUSE
      Water filling system not connected.
      SOLUTION
      Connect the water filling system to the sterilizer. (see Instructions For Use).

      POSSIBLE CAUSE
      When the water filling system attempted to fill the tank, water was temporarily unavailable.
      SOLUTION
      Since the water tank filling is attempted only once in-between cycle execution, this event inhibits water feeding. Switch the sterilizer OFF and then ON again.
      Check the external water supply system.
      Check for water leaks from the sterilizer.

      POSSIBLE CAUSE
      Faulty MIN water level sensor in the clean water tank
      SOLUTION
      Contact an authorized W&H service partner.
    • The sterilization (PROCESS) phase of a sterilization cycle was longer than expected.
      POSSIBLE CAUSE
      The chamber temperature dropped below the minimum threshold and the software performed a successful recovery
      SOLUTION
      Wait for cycle completion. If the problem occurs frequently, contact an authorized W&H service partner.
    • Warning about consumable replacement.
      POSSIBLE CAUSE
      A consumable needs to be replaced.
      SOLUTION
      Order the requested consumable (door seal and HEPA/bacteriological filter) and replace it. See the chapter “Maintenance” in the Instructions for Use.
    • Which is the maximum noise level of Lina?
      The max. noise level of Lina is 65.5 dB.
    • Which water quality should I use for my Lexa Plus sterilizer?
      The water quality for sterilizers is internationally specified by standards and directives. The reasons for this are that your sterilizer can be seriously damaged by it or the sterilization can be jeopardised. Consequently, only water with conductivity of less than 10 µS/cm in North America and 15 µS/cm for the rest of the world should be used for your W&H sterilizer. The Multidem system and OSMO are especially designed to prepare suitable water (see chapter “Water quality” in the Instructions for Use).
    • Do I need to carry out periodic testing on my W&H Sterilizer?
      All W&H sterilizers features test cycles (B&D/Helix test, Vacuum test). Compulsory and frequency of testing are regulated by local/national guidelines.
  • Lexa (23)
    • What is validation?
      Validation is a testing procedure carried out by an official authority, proving the effectiveness of your sterilizer. Compulsories and frequency of validation are regulated by local/national guidelines.
    • Do I need to document the results of all periodic tests?
      W&H recommends recording all periodic tests, repairs and modifications on the sterilizer in a logbook including date and signature of the person who carried out the test or other activity. Compulsoriness of recording is regulated by local/national guidelines.
    • How long should I archive the documentation of regular tests?
      Keep the results according to your country/regional specific laws and guidelines. Those records can be of assistance in case of service as well.
    • Does my sterilizer need any periodic qualification/validation?
      Validation generally comprises a range of tests defined in internationally recognised standards. These tests begin for every device with the factory tests at W&H. In addition, corresponding documentation is included with your device. Prior to commissioning the device at your premises, the technician performs further checks to ensure the device functions correctly. Then, depending on the national/regional laws and directives, the device must be subjected to a so-called renewed performance qualification at regular intervals. For further information, please contact your dealer.
    • Whom should I contact to validate and maintain my sterilizer?
      Validation shall be carried out by an official authority. Maintenance tasks shall be carried out by a qualified and authorized technician.
    • How do I change consumable components on my sterilizer?
      Consumable replacement instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu; • in the Consumables & Accessories and Video Tutorial section of this web site.
    • How do I clean the water tanks and what products should I use?
      Water tank cleaning instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu;
      • in the Consumables & Accessories and Video Tutorial section of this web site.
    • Should I pouch wrap my instruments and how long can I store them after sterilization?
      To ensure that your instruments are stored in a sterile state from their successful sterilization until they are used, W&H recommends wrapping them in suitable sterile barrier systems before sterilization. The recommended storage period can be found in the recommendations of the wrapping material manufacturer. For further information, please contact your dealer.
    • The sterilizer remains switched OFF.
      POSSIBLE CAUSE
      The main switch or network circuit breaker is OFF.
      SOLUTION
      Activate the main switch or network circuit breaker (ON).

      POSSIBLE CAUSE
      No voltage at the socket.
      SOLUTION
      Check the building electrical supply.

      POSSIBLE CAUSE
      The power cord is not connected properly
      SOLUTION
      Check and connect the power cord properly
    • Water is leaking at the front of the sterilizer.
      POSSIBLE CAUSE
      Leaks through the chamber door seal.
      SOLUTION
      Clean or replace the door seal. Clean the door surface facing the chamber.

      POSSIBLE CAUSE
      Internal leak.
      SOLUTIONS
      Contact an authorized W&H service partner.
    • At the end of the cycle, there is residual water in the chamber
      POSSIBLE CAUSE
      Sterilizer not properly levelled
      SOLUTION
      Place the sterilizer on a flat, levelled surface.

      POSSIBLE CAUSE
      Overloaded chamber
      SOLUTION
      Comply with the maximum load weight limits for each type of load. Always use the chamber rack for trays and cassettes.

      POSSIBLE CAUSE
      Chamber filter clogged
      SOLUTION
      Remove and clean the chamber filter.

      POSSIBLE CAUSE
      Load incorrectly placed
      SOLUTION
      Follow the recommendations as listed in chapter “Load maintenance and preparation” in the Instructions for Use.
    • The sterilizer enters into “Standby mode” immediately after being switched on.
      POSSIBLE CAUSE
      The unit was turned off while in standby mode.
      SOLUTION
      Press the “Standby mode” button to exit.
    • When starting a cycle, the chamber door locks but re-opens immediately. The “Open the door” message appears.
      POSSIBLE CAUSE
      Door seal not properly placed.
      SOLUTION
      Ensure that the door seal is correctly inserted around the whole circumference.

      POSSIBLE CAUSE
      Door jammed by external objects or by the load itself
      SOLUTION
      Remove any objects interfering with the chamber door. Check for interference between the door and the chamber furniture and/or the load.
    • Stains, spots or colour change on instruments.
      POSSIBLE CAUSE
      Instruments rinsed with tap water and not dried before sterilization.
      SOLUTION
      Ensure that instruments are rinsed with distilled or demineralized water and completely dry before they are placed in the sterilizer.

      POSSIBLE CAUSE
      Use of water of poor quality or water containing chemical substances
      SOLUTION
      Drain both water tanks. Use good quality water (see chapter “Water quality” in the Instructions for Use).

      POSSIBLE CAUSE
      Organic or chemical residues on the instruments
      SOLUTION
      Clean, rinse and dry instruments before placing them in the sterilizer (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Dirt in chamber, trays, tray rack.
      SOLUTION
      Clean the chamber and wash the chamber furniture

      POSSIBLE CAUSE
      Contact between instruments of different materials
      SOLUTION
      Ensure that instruments of different materials do not touch each other (aluminum, carbon or stainless steel, etc.); place them on different trays or cassettes or pouch them (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Scale deposits on the chamber
      SOLUTION
      Clean the chamber and use good quality water (see chapter “Water quality” in the Instructions for Use).
    • No cycles are stored in the cycle history menu
      POSSIBLE CAUSE
      An electronic board was replaced when serviced.
      SOLUTION
      The memory of the old board cannot be restored. Consult the cycle history in the USB pen drive.
    • Warning about saving to the USB (HTML and SCL files)
      POSSIBLE CAUSE
      The USB pen drive is disconnected or full.
      SOLUTION
      Check presence and condition of the USB pen drive. If the problem persist, contact an authorized W&H service partner.
    • The cycle report printer does not work.
      POSSIBLE CAUSE
      Printer not properly connected or not powered
      SOLUTION
      Check the data and the power connection to the printer.
    • The sterilizer is connected to an automated water supply system, there is no clean water in the tank and the automatic water filling does not fill the water.
      POSSIBLE CAUSE
      Water filling system not connected.
      SOLUTION
      Connect the water filling system to the sterilizer. (see Instructions For Use).

      POSSIBLE CAUSE
      When the water filling system attempted to fill the tank, water was temporarily unavailable.
      SOLUTION
      Since the water tank filling is attempted only once in-between cycle execution, this event inhibits water feeding. Switch the sterilizer OFF and then ON again.
      Check the external water supply system.
      Check for water leaks from the sterilizer.

      POSSIBLE CAUSE
      Faulty MIN water level sensor in the clean water tank
      SOLUTION
      Contact an authorized W&H service partner.
    • The sterilization (PROCESS) phase of a sterilization cycle was longer than expected.
      POSSIBLE CAUSE
      The chamber temperature dropped below the minimum threshold and the software performed a successful recovery
      SOLUTION
      Wait for cycle completion. If the problem occurs frequently, contact an authorized W&H service partner.
    • Warning about consumable replacement.
      POSSIBLE CAUSE
      A consumable needs to be replaced.
      SOLUTION
      Order the requested consumable (door seal and HEPA/bacteriological filter) and replace it. See the chapter “Maintenance” in the Instructions for Use.
    • Which water quality should I use for my sterilizer?
      The water quality for sterilizers is internationally specified by standards and directives. The reasons for this are that your sterilizer can be seriously damaged by it or the sterilization can be jeopardized. Consequently, only water with conductivity of less than 10 µS/cm should be used for your W&H sterilizer. The Multidem system is especially suited to preparing suitable water (see chapter “Water quality” in the Instructions for Use).
    • What is the maximum noise level of the Lexa sterilizer?
      The max. noise level of Lexa is 65 dB.
    • Do I need to carry out periodic testing on my W&H Sterilizer?
      All W&H sterilizers features test cycles (B&D/Helix test, Vacuum test). Compulsory and frequency of testing are regulated by local/national guidelines.
  • Lyla (24)
    • What is validation?
      Validation is a testing procedure carried out by an official authority, proving the effectiveness of your sterilizer. Compulsories and frequency of validation are regulated by local/national guidelines.
    • Do I need to document the results of all periodic tests?
      W&H recommends recording all periodic tests, repairs and modifications on the sterilizer in a logbook including date and signature of the person who carried out the test or other activity. Compulsoriness of recording is regulated by local/national guidelines.
    • How long should I archive the documentation of regular tests?
      Keep the results according to your country/regional specific laws and guidelines. Those records can be of assistance in case of service as well.
    • Does my sterilizer need any periodic qualification/validation?
      Validation generally comprises a range of tests defined in internationally recognised standards. These tests begin for every device with the factory tests at W&H. In addition, corresponding documentation is included with your device. Prior to commissioning the device at your premises, the technician performs further checks to ensure the device functions correctly. Then, depending on the national/regional laws and directives, the device must be subjected to a so-called renewed performance qualification at regular intervals. For further information, please contact your dealer.
    • Whom should I contact to validate and maintain my sterilizer?
      Validation shall be carried out by an official authority. Maintenance tasks shall be carried out by a qualified and authorized technician.
    • How do I change consumable components on my sterilizer?
      Consumable replacement instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu; • in the Consumables & Accessories and Video Tutorial section of this web site.
    • How do I clean the water tanks and what products should I use?
      Water tank cleaning instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu;
      • in the Consumables & Accessories and Video Tutorial section of this web site.
    • Should I pouch wrap my instruments and how long can I store them after sterilization?
      To ensure that your instruments are stored in a sterile state from their successful sterilization until they are used, W&H recommends wrapping them in suitable sterile barrier systems before sterilization. The recommended storage period can be found in the recommendations of the wrapping material manufacturer. For further information, please contact your dealer.
    • The sterilizer remains switched OFF.
      POSSIBLE CAUSE
      The main switch or network circuit breaker is OFF.
      SOLUTION
      Activate the main switch or network circuit breaker (ON).

      POSSIBLE CAUSE
      No voltage at the socket.
      SOLUTION
      Check the building electrical supply.

      POSSIBLE CAUSE
      The power cord is not connected properly
      SOLUTION
      Check and connect the power cord properly
    • Water is leaking at the front of the sterilizer.
      POSSIBLE CAUSE
      Leaks through the chamber door seal.
      SOLUTION
      Clean or replace the door seal. Clean the door surface facing the chamber.

      POSSIBLE CAUSE
      Internal leak.
      SOLUTIONS
      Contact an authorized W&H service partner.
    • At the end of the cycle, there is residual water in the chamber
      POSSIBLE CAUSE
      Sterilizer not properly levelled
      SOLUTION
      Place the sterilizer on a flat, levelled surface.

      POSSIBLE CAUSE
      Overloaded chamber
      SOLUTION
      Comply with the maximum load weight limits for each type of load. Always use the chamber rack for trays and cassettes.

      POSSIBLE CAUSE
      Chamber filter clogged
      SOLUTION
      Remove and clean the chamber filter.

      POSSIBLE CAUSE
      Load incorrectly placed
      SOLUTION
      Follow the recommendations as listed in chapter “Load maintenance and preparation” in the Instructions for Use.
    • The sterilizer enters into “Standby mode” immediately after being switched on.
      POSSIBLE CAUSE
      The unit was turned off while in standby mode.
      SOLUTION
      Press the “Standby mode” button to exit.
    • When starting a cycle, the chamber door locks but re-opens immediately. The “Open the door” message appears.
      POSSIBLE CAUSE
      Door seal not properly placed.
      SOLUTION
      Ensure that the door seal is correctly inserted around the whole circumference.

      POSSIBLE CAUSE
      Door jammed by external objects or by the load itself
      SOLUTION
      Remove any objects interfering with the chamber door. Check for interference between the door and the chamber furniture and/or the load.
    • Stains, spots or colour change on instruments.
      POSSIBLE CAUSE
      Instruments rinsed with tap water and not dried before sterilization.
      SOLUTION
      Ensure that instruments are rinsed with distilled or demineralized water and completely dry before they are placed in the sterilizer.

      POSSIBLE CAUSE
      Use of water of poor quality or water containing chemical substances
      SOLUTION
      Drain both water tanks. Use good quality water (see chapter “Water quality” in the Instructions for Use).

      POSSIBLE CAUSE
      Organic or chemical residues on the instruments
      SOLUTION
      Clean, rinse and dry instruments before placing them in the sterilizer (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Dirt in chamber, trays, tray rack.
      SOLUTION
      Clean the chamber and wash the chamber furniture

      POSSIBLE CAUSE
      Contact between instruments of different materials
      SOLUTION
      Ensure that instruments of different materials do not touch each other (aluminum, carbon or stainless steel, etc.); place them on different trays or cassettes or pouch them (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Scale deposits on the chamber
      SOLUTION
      Clean the chamber and use good quality water (see chapter “Water quality” in the Instructions for Use).
    • No cycles are stored in the cycle history menu
      POSSIBLE CAUSE
      An electronic board was replaced when serviced.
      SOLUTION
      The memory of the old board cannot be restored. Consult the cycle history in the USB pen drive.
    • Warning about saving to the USB (HTML and SCL files)
      POSSIBLE CAUSE
      The USB pen drive is disconnected or full.
      SOLUTION
      Check presence and condition of the USB pen drive. If the problem persist, contact an authorized W&H service partner.
    • Warning about programmed maintenance.
      POSSIBLE CAUSE
      The maintenance program needs to be carried out.
      SOLUTION
      Contact an authorized W&H service partner.
    • The cycle report printer does not work.
      POSSIBLE CAUSE
      Printer not properly connected or not powered
      SOLUTION
      Check the data and the power connection to the printer.
    • The sterilizer is connected to an automated water supply system, there is no clean water in the tank and the automatic water filling does not fill the water.
      POSSIBLE CAUSE
      Water filling system not connected.
      SOLUTION
      Connect the water filling system to the sterilizer. (see Instructions For Use).

      POSSIBLE CAUSE
      When the water filling system attempted to fill the tank, water was temporarily unavailable.
      SOLUTION
      Since the water tank filling is attempted only once in-between cycle execution, this event inhibits water feeding. Switch the sterilizer OFF and then ON again.
      Check the external water supply system.
      Check for water leaks from the sterilizer.

      POSSIBLE CAUSE
      Faulty MIN water level sensor in the clean water tank
      SOLUTION
      Contact an authorized W&H service partner.
    • The sterilization (PROCESS) phase of a sterilization cycle was longer than expected.
      POSSIBLE CAUSE
      The chamber temperature dropped below the minimum threshold and the software performed a successful recovery
      SOLUTION
      Wait for cycle completion. If the problem occurs frequently, contact an authorized W&H service partner.
    • Warning about consumable replacement.
      POSSIBLE CAUSE
      A consumable needs to be replaced.
      SOLUTION
      Order the requested consumable (door seal and HEPA/bacteriological filter) and replace it. See the chapter “Maintenance” in the Instructions for Use.
    • Which is the maximum noise level of Lyla?
      The max. noise level of Lyla is 65.5 dB.
    • Which water quality should I use for my Lexa Plus sterilizer?
      The water quality for sterilizers is internationally specified by standards and directives. The reasons for this are that your sterilizer can be seriously damaged by it or the sterilization can be jeopardised. Consequently, only water with conductivity of less than 10 µS/cm in North America and 15 µS/cm for the rest of the world should be used for your W&H sterilizer. The Multidem system and OSMO are especially designed to prepare suitable water (see chapter “Water quality” in the Instructions for Use).
    • Do I need to carry out periodic testing on my W&H Sterilizer?
      All W&H sterilizers features test cycles (B&D/Helix test, Vacuum test). Compulsory and frequency of testing are regulated by local/national guidelines.
  • Lexa Plus (24)
    • What is validation?
      Validation is a testing procedure carried out by an official authority, proving the effectiveness of your sterilizer. Compulsories and frequency of validation are regulated by local/national guidelines.
    • Do I need to document the results of all periodic tests?
      W&H recommends recording all periodic tests, repairs and modifications on the sterilizer in a logbook including date and signature of the person who carried out the test or other activity. Compulsoriness of recording is regulated by local/national guidelines.
    • How long should I archive the documentation of regular tests?
      Keep the results according to your country/regional specific laws and guidelines. Those records can be of assistance in case of service as well.
    • Does my sterilizer need any periodic qualification/validation?
      Validation generally comprises a range of tests defined in internationally recognised standards. These tests begin for every device with the factory tests at W&H. In addition, corresponding documentation is included with your device. Prior to commissioning the device at your premises, the technician performs further checks to ensure the device functions correctly. Then, depending on the national/regional laws and directives, the device must be subjected to a so-called renewed performance qualification at regular intervals. For further information, please contact your dealer.
    • Whom should I contact to validate and maintain my sterilizer?
      Validation shall be carried out by an official authority. Maintenance tasks shall be carried out by a qualified and authorized technician.
    • How do I change consumable components on my sterilizer?
      Consumable replacement instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu; • in the Consumables & Accessories and Video Tutorial section of this web site.
    • How do I clean the water tanks and what products should I use?
      Water tank cleaning instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu;
      • in the Consumables & Accessories and Video Tutorial section of this web site.
    • Should I pouch wrap my instruments and how long can I store them after sterilization?
      To ensure that your instruments are stored in a sterile state from their successful sterilization until they are used, W&H recommends wrapping them in suitable sterile barrier systems before sterilization. The recommended storage period can be found in the recommendations of the wrapping material manufacturer. For further information, please contact your dealer.
    • The sterilizer remains switched OFF.
      POSSIBLE CAUSE
      The main switch or network circuit breaker is OFF.
      SOLUTION
      Activate the main switch or network circuit breaker (ON).

      POSSIBLE CAUSE
      No voltage at the socket.
      SOLUTION
      Check the building electrical supply.

      POSSIBLE CAUSE
      The power cord is not connected properly
      SOLUTION
      Check and connect the power cord properly
    • Water is leaking at the front of the sterilizer.
      POSSIBLE CAUSE
      Leaks through the chamber door seal.
      SOLUTION
      Clean or replace the door seal. Clean the door surface facing the chamber.

      POSSIBLE CAUSE
      Internal leak.
      SOLUTIONS
      Contact an authorized W&H service partner.
    • At the end of the cycle, there is residual water in the chamber
      POSSIBLE CAUSE
      Sterilizer not properly levelled
      SOLUTION
      Place the sterilizer on a flat, levelled surface.

      POSSIBLE CAUSE
      Overloaded chamber
      SOLUTION
      Comply with the maximum load weight limits for each type of load. Always use the chamber rack for trays and cassettes.

      POSSIBLE CAUSE
      Chamber filter clogged
      SOLUTION
      Remove and clean the chamber filter.

      POSSIBLE CAUSE
      Load incorrectly placed
      SOLUTION
      Follow the recommendations as listed in chapter “Load maintenance and preparation” in the Instructions for Use.
    • The sterilizer enters into “Standby mode” immediately after being switched on.
      POSSIBLE CAUSE
      The unit was turned off while in standby mode.
      SOLUTION
      Press the “Standby mode” button to exit.
    • When starting a cycle, the chamber door locks but re-opens immediately. The “Open the door” message appears.
      POSSIBLE CAUSE
      Door seal not properly placed.
      SOLUTION
      Ensure that the door seal is correctly inserted around the whole circumference.

      POSSIBLE CAUSE
      Door jammed by external objects or by the load itself
      SOLUTION
      Remove any objects interfering with the chamber door. Check for interference between the door and the chamber furniture and/or the load.
    • Stains, spots or colour change on instruments.
      POSSIBLE CAUSE
      Instruments rinsed with tap water and not dried before sterilization.
      SOLUTION
      Ensure that instruments are rinsed with distilled or demineralized water and completely dry before they are placed in the sterilizer.

      POSSIBLE CAUSE
      Use of water of poor quality or water containing chemical substances
      SOLUTION
      Drain both water tanks. Use good quality water (see chapter “Water quality” in the Instructions for Use).

      POSSIBLE CAUSE
      Organic or chemical residues on the instruments
      SOLUTION
      Clean, rinse and dry instruments before placing them in the sterilizer (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Dirt in chamber, trays, tray rack.
      SOLUTION
      Clean the chamber and wash the chamber furniture

      POSSIBLE CAUSE
      Contact between instruments of different materials
      SOLUTION
      Ensure that instruments of different materials do not touch each other (aluminum, carbon or stainless steel, etc.); place them on different trays or cassettes or pouch them (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Scale deposits on the chamber
      SOLUTION
      Clean the chamber and use good quality water (see chapter “Water quality” in the Instructions for Use).
    • No cycles are stored in the cycle history menu
      POSSIBLE CAUSE
      An electronic board was replaced when serviced.
      SOLUTION
      The memory of the old board cannot be restored. Consult the cycle history in the USB pen drive.
    • Warning about saving to the USB (HTML and SCL files)
      POSSIBLE CAUSE
      The USB pen drive is disconnected or full.
      SOLUTION
      Check presence and condition of the USB pen drive. If the problem persist, contact an authorized W&H service partner.
    • Warning about programmed maintenance.
      POSSIBLE CAUSE
      The maintenance program needs to be carried out.
      SOLUTION
      Contact an authorized W&H service partner.
    • The cycle report printer does not work.
      POSSIBLE CAUSE
      Printer not properly connected or not powered
      SOLUTION
      Check the data and the power connection to the printer.
    • The sterilizer is connected to an automated water supply system, there is no clean water in the tank and the automatic water filling does not fill the water.
      POSSIBLE CAUSE
      Water filling system not connected.
      SOLUTION
      Connect the water filling system to the sterilizer. (see Instructions For Use).

      POSSIBLE CAUSE
      When the water filling system attempted to fill the tank, water was temporarily unavailable.
      SOLUTION
      Since the water tank filling is attempted only once in-between cycle execution, this event inhibits water feeding. Switch the sterilizer OFF and then ON again.
      Check the external water supply system.
      Check for water leaks from the sterilizer.

      POSSIBLE CAUSE
      Faulty MIN water level sensor in the clean water tank
      SOLUTION
      Contact an authorized W&H service partner.
    • The sterilization (PROCESS) phase of a sterilization cycle was longer than expected.
      POSSIBLE CAUSE
      The chamber temperature dropped below the minimum threshold and the software performed a successful recovery
      SOLUTION
      Wait for cycle completion. If the problem occurs frequently, contact an authorized W&H service partner.
    • Warning about consumable replacement.
      POSSIBLE CAUSE
      A consumable needs to be replaced.
      SOLUTION
      Order the requested consumable (door seal and HEPA/bacteriological filter) and replace it. See the chapter “Maintenance” in the Instructions for Use.
    • What is the maximum noise level of the Lexa Plus sterilizer?
      The max. noise level of the Lexa Plus is 70 dB.
    • Which water quality should I use for my Lexa Plus sterilizer?
      The water quality for sterilizers is internationally specified by standards and directives. The reasons for this are that your sterilizer can be seriously damaged by it or the sterilization can be jeopardised. Consequently, only water with conductivity of less than 10 µS/cm in North America and 15 µS/cm for the rest of the world should be used for your W&H sterilizer. The Multidem system and OSMO are especially designed to prepare suitable water (see chapter “Water quality” in the Instructions for Use).
    • Do I need to carry out periodic testing on my W&H Sterilizer?
      All W&H sterilizers features test cycles (B&D/Helix test, Vacuum test). Compulsory and frequency of testing are regulated by local/national guidelines.
  • Lexa Mini (11)
    • What is validation?
      Validation is a testing procedure carried out by an official authority, proving the effectiveness of your sterilizer. Compulsories and frequency of validation are regulated by local/national guidelines.
    • Do I need to document the results of all periodic tests?
      W&H recommends recording all periodic tests, repairs and modifications on the sterilizer in a logbook including date and signature of the person who carried out the test or other activity. Compulsoriness of recording is regulated by local/national guidelines.
    • How long should I archive the documentation of regular tests?
      Keep the results according to your country/regional specific laws and guidelines. Those records can be of assistance in case of service as well.
    • Does my sterilizer need any periodic qualification/validation?
      Validation generally comprises a range of tests defined in internationally recognised standards. These tests begin for every device with the factory tests at W&H. In addition, corresponding documentation is included with your device. Prior to commissioning the device at your premises, the technician performs further checks to ensure the device functions correctly. Then, depending on the national/regional laws and directives, the device must be subjected to a so-called renewed performance qualification at regular intervals. For further information, please contact your dealer.
    • Whom should I contact to validate and maintain my sterilizer?
      Validation shall be carried out by an official authority. Maintenance tasks shall be carried out by a qualified and authorized technician.
    • Should I pouch wrap my instruments and how long can I store them after sterilization?
      To ensure that your instruments are stored in a sterile state from their successful sterilization until they are used, W&H recommends wrapping them in suitable sterile barrier systems before sterilization. The recommended storage period can be found in the recommendations of the wrapping material manufacturer. For further information, please contact your dealer.
    • Which water quality should I use for my Lexa Plus sterilizer?
      The water quality for sterilizers is internationally specified by standards and directives. The reasons for this are that your sterilizer can be seriously damaged by it or the sterilization can be jeopardised. Consequently, only water with conductivity of less than 10 µS/cm in North America and 15 µS/cm for the rest of the world should be used for your W&H sterilizer. The Multidem system and OSMO are especially designed to prepare suitable water (see chapter “Water quality” in the Instructions for Use).
    • Do I need to carry out periodic testing on my W&H Sterilizer?
      All W&H sterilizers features test cycles (B&D/Helix test, Vacuum test). Compulsory and frequency of testing are regulated by local/national guidelines.
    • How do I clean the water tank and what products should I use?
      Water tank cleaning instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available: • in the sterilizer, in the maintenance section of the menu.
    • What is the maximum noise level of the Lisa Mini sterilizer?
      The max. noise level of Lisa Mini is 64 dB.
    • How do I change consumable components on my sterilizer?
      Consumable replacement instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available: • in the sterilizer, in the maintenance section of the menu.
  • Lisa (24)
    • What is validation?
      Validation is a testing procedure carried out by an official authority, proving the effectiveness of your sterilizer. Compulsories and frequency of validation are regulated by local/national guidelines.
    • Do I need to document the results of all periodic tests?
      W&H recommends recording all periodic tests, repairs and modifications on the sterilizer in a logbook including date and signature of the person who carried out the test or other activity. Compulsoriness of recording is regulated by local/national guidelines.
    • How long should I archive the documentation of regular tests?
      Keep the results according to your country/regional specific laws and guidelines. Those records can be of assistance in case of service as well.
    • Does my sterilizer need any periodic qualification/validation?
      Validation generally comprises a range of tests defined in internationally recognised standards. These tests begin for every device with the factory tests at W&H. In addition, corresponding documentation is included with your device. Prior to commissioning the device at your premises, the technician performs further checks to ensure the device functions correctly. Then, depending on the national/regional laws and directives, the device must be subjected to a so-called renewed performance qualification at regular intervals. For further information, please contact your dealer.
    • Whom should I contact to validate and maintain my sterilizer?
      Validation shall be carried out by an official authority. Maintenance tasks shall be carried out by a qualified and authorized technician.
    • How do I change consumable components on my sterilizer?
      Consumable replacement instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu; • in the Consumables & Accessories and Video Tutorial section of this web site.
    • How do I clean the water tanks and what products should I use?
      Water tank cleaning instructions are provided in the Instructions for Use, chapter “Maintenance”. In addition, a video description is available:
      • in the sterilizer, in the maintenance section of the menu;
      • in the Consumables & Accessories and Video Tutorial section of this web site.
    • Should I pouch wrap my instruments and how long can I store them after sterilization?
      To ensure that your instruments are stored in a sterile state from their successful sterilization until they are used, W&H recommends wrapping them in suitable sterile barrier systems before sterilization. The recommended storage period can be found in the recommendations of the wrapping material manufacturer. For further information, please contact your dealer.
    • The sterilizer remains switched OFF.
      POSSIBLE CAUSE
      The main switch or network circuit breaker is OFF.
      SOLUTION
      Activate the main switch or network circuit breaker (ON).

      POSSIBLE CAUSE
      No voltage at the socket.
      SOLUTION
      Check the building electrical supply.

      POSSIBLE CAUSE
      The power cord is not connected properly
      SOLUTION
      Check and connect the power cord properly
    • Water is leaking at the front of the sterilizer.
      POSSIBLE CAUSE
      Leaks through the chamber door seal.
      SOLUTION
      Clean or replace the door seal. Clean the door surface facing the chamber.

      POSSIBLE CAUSE
      Internal leak.
      SOLUTIONS
      Contact an authorized W&H service partner.
    • At the end of the cycle, there is residual water in the chamber
      POSSIBLE CAUSE
      Sterilizer not properly levelled
      SOLUTION
      Place the sterilizer on a flat, levelled surface.

      POSSIBLE CAUSE
      Overloaded chamber
      SOLUTION
      Comply with the maximum load weight limits for each type of load. Always use the chamber rack for trays and cassettes.

      POSSIBLE CAUSE
      Chamber filter clogged
      SOLUTION
      Remove and clean the chamber filter.

      POSSIBLE CAUSE
      Load incorrectly placed
      SOLUTION
      Follow the recommendations as listed in chapter “Load maintenance and preparation” in the Instructions for Use.
    • The sterilizer enters into “Standby mode” immediately after being switched on.
      POSSIBLE CAUSE
      The unit was turned off while in standby mode.
      SOLUTION
      Press the “Standby mode” button to exit.
    • When starting a cycle, the chamber door locks but re-opens immediately. The “Open the door” message appears.
      POSSIBLE CAUSE
      Door seal not properly placed.
      SOLUTION
      Ensure that the door seal is correctly inserted around the whole circumference.

      POSSIBLE CAUSE
      Door jammed by external objects or by the load itself
      SOLUTION
      Remove any objects interfering with the chamber door. Check for interference between the door and the chamber furniture and/or the load.
    • Stains, spots or colour change on instruments.
      POSSIBLE CAUSE
      Instruments rinsed with tap water and not dried before sterilization.
      SOLUTION
      Ensure that instruments are rinsed with distilled or demineralized water and completely dry before they are placed in the sterilizer.

      POSSIBLE CAUSE
      Use of water of poor quality or water containing chemical substances
      SOLUTION
      Drain both water tanks. Use good quality water (see chapter “Water quality” in the Instructions for Use).

      POSSIBLE CAUSE
      Organic or chemical residues on the instruments
      SOLUTION
      Clean, rinse and dry instruments before placing them in the sterilizer (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Dirt in chamber, trays, tray rack.
      SOLUTION
      Clean the chamber and wash the chamber furniture

      POSSIBLE CAUSE
      Contact between instruments of different materials
      SOLUTION
      Ensure that instruments of different materials do not touch each other (aluminum, carbon or stainless steel, etc.); place them on different trays or cassettes or pouch them (see chapter “Load maintenance and preparation” in the Instructions for Use).

      POSSIBLE CAUSE
      Scale deposits on the chamber
      SOLUTION
      Clean the chamber and use good quality water (see chapter “Water quality” in the Instructions for Use).
    • No cycles are stored in the cycle history menu
      POSSIBLE CAUSE
      An electronic board was replaced when serviced.
      SOLUTION
      The memory of the old board cannot be restored. Consult the cycle history in the USB pen drive.
    • Warning about saving to the USB (HTML and SCL files)
      POSSIBLE CAUSE
      The USB pen drive is disconnected or full.
      SOLUTION
      Check presence and condition of the USB pen drive. If the problem persist, contact an authorized W&H service partner.
    • Warning about programmed maintenance.
      POSSIBLE CAUSE
      The maintenance program needs to be carried out.
      SOLUTION
      Contact an authorized W&H service partner.
    • The cycle report printer does not work.
      POSSIBLE CAUSE
      Printer not properly connected or not powered
      SOLUTION
      Check the data and the power connection to the printer.
    • The sterilizer is connected to an automated water supply system, there is no clean water in the tank and the automatic water filling does not fill the water.
      POSSIBLE CAUSE
      Water filling system not connected.
      SOLUTION
      Connect the water filling system to the sterilizer. (see Instructions For Use).

      POSSIBLE CAUSE
      When the water filling system attempted to fill the tank, water was temporarily unavailable.
      SOLUTION
      Since the water tank filling is attempted only once in-between cycle execution, this event inhibits water feeding. Switch the sterilizer OFF and then ON again.
      Check the external water supply system.
      Check for water leaks from the sterilizer.

      POSSIBLE CAUSE
      Faulty MIN water level sensor in the clean water tank
      SOLUTION
      Contact an authorized W&H service partner.
    • The sterilization (PROCESS) phase of a sterilization cycle was longer than expected.
      POSSIBLE CAUSE
      The chamber temperature dropped below the minimum threshold and the software performed a successful recovery
      SOLUTION
      Wait for cycle completion. If the problem occurs frequently, contact an authorized W&H service partner.
    • Warning about consumable replacement.
      POSSIBLE CAUSE
      A consumable needs to be replaced.
      SOLUTION
      Order the requested consumable (door seal and HEPA/bacteriological filter) and replace it. See the chapter “Maintenance” in the Instructions for Use.
    • What is the maximum noise level of the Lisa sterilizer?
      The max. noise level of Lisa 2019 is 64.3 dB.
    • Which water quality should I use for my Lexa Plus sterilizer?
      The water quality for sterilizers is internationally specified by standards and directives. The reasons for this are that your sterilizer can be seriously damaged by it or the sterilization can be jeopardised. Consequently, only water with conductivity of less than 10 µS/cm in North America and 15 µS/cm for the rest of the world should be used for your W&H sterilizer. The Multidem system and OSMO are especially designed to prepare suitable water (see chapter “Water quality” in the Instructions for Use).
    • Do I need to carry out periodic testing on my W&H Sterilizer?
      All W&H sterilizers features test cycles (B&D/Helix test, Vacuum test). Compulsory and frequency of testing are regulated by local/national guidelines.

Air Motor

  • Does the air motor need to be greased?
    Yes, the air motor must be lubricated as described in the "Hygiene and care" section of the instructions for use. Please make sure that the controll ring is positioned either to forward or reverse direction.

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