Lexa sterilizer
Discover the Lexa sterilizer for yourself!
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Sterilization on a high standard
Built to offer more of all that counts in every day medical infection control.
Your sterilization process deserves Lexa!- Incredible efficiency: Large chamber capacity of 7.4 gallons and short cycle times, including excellent load drying.
- Incredible flexibility: Lexa comes with 4 large trays along with a unique rack providing larger loading surface and more loading options.
- Incredible protection: Automatic digital cycle recording on USB stick.
- Incredible speed: Lexa offers versatile program options for several loads in order to reduce overall cycle duration.
- Incredible usability: User-friendly interface and high-end 4.3” color touchscreen for simple navigation to all sterilization option.
- Incredible standards: Closed-door vacuum-assisted drying for excellent load drying and single use water management.
Your advantages at a glance
- User-friendly interface and high-end colour touchscreen for simple navigation to all sterilization option
- Customizable drying time
- Large capacity sterilizer chamber with unique tray and exclusive design
- Versatile sterilization program options with short cycle times
- Superior vacuum-assisted drying
- Meets stringent hygiene standards, including dynamic pulsed air removal, closed door drying and single-use water management
- Easy maintenance – Lexa does not require periodic execution of cleaning cycles
- Programmable cycle start
- Excellent value for money
- Automatic digital cycle recording on USB stick
- User authentication and load release (optional)
- Barcode label printing (optional)
Lexa sterilizer
supplied with autofill & autodrain, tray rack, 4 aluminium trays, drain tube, tray holder, USB drive & emergency door opening tool
Warranty details: 2 years or 2,000 cycles - whichever comes first.Lexa MN-111
110 V
REF 19943401Chamber size 28 l
100–125 V AC; 50/60 Hz; 12 A Single PhaseLexa MN-111
220 V
REF 19943101Chamber size 28 l
200–240 V AC; 50/60 Hz 10 A Single PhaseDownload Area
FAQs
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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. more
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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. more
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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. more
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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. more
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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. more
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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. more -
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. more -
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. more
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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 more -
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. more -
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. more -
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. more -
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. more -
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). more -
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. more -
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. more -
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. more -
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. more -
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. more -
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. more -
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). more
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What is the maximum noise level of the Lexa sterilizer?
The max. noise level of Lexa is 65 dB. more
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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. more
Instructions for use
Find all languages of the Update Hygiene and Maintenance (EN ISO 17664:2017) in the Download Centre.
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Lexa sterilization programs
Sterilization cycle Unwrapped Pouches Medium Load
Pouches Large Load Pouches & Wrapped Cassettes Wrapped
Cassettes
Low
TemperatureTemperature: 132°C (270°F) 132°C (270°F) 132°C (270°F) 132°C (270°F) 132°C (270°F) 121°C (250°F) Holding time (minutes): 4’ 4’ 4’ 4’ 4’ 30’ Total cycle duration (minutes) including drying*: 26’–39’ 43’–53’ 48’–58’ 53'-64' 58'-71' 73’–79’ Max. load (excluding trays): 8.1 kg (18 lbs) 1.4 kg (3 lbs) 2.7 kg (6 lbs) 5.0 kg (11 lbs) 6.4 kg (14 lbs) 2.3 & 2 kg (5 & 4.4 lbs) including trays
Items supplied with: chamber rack, 4 larger trays, tray holder, drain tube, USB drive.
* Cycle times are approximate and may vary depending on voltage and instrument loads.
Trade name: Lexa 110 V Lexa 220 V Type: MN-111 Chamber size: 28 l (7.4 gal) Power supply: 100–125 V AC; 50/60 Hz; 12 A Single Phase
200–240 V AC; 50/60 Hz 10 A Single Phase
Overall dimension
(width x height x depth):490 x 452 x 616 mm (19.3“ x 17.8“ x 24.3“) Weight: 48 kg (105.8 lbs) Main / Used water tanks: 6.4/6.7 l (1.7/1.8 gal) Connection types: 5 USB ports, 1 Ethernet port Lexa sterilizers were designed, certified and validated according to the following standards and directives: N°2017/745 Medical Device Regulation EN 13060 Small steam sterilizer IEC 61326-1 Electromagnetic compatibility IEC 61010-1 Safety requirements
IEC 61010-2-040 Specific requirements for steam sterilizer
IEC 61770 Back syphonage
ASME* Boiler and pressure vessel code
ANSI/AAMI ST55 Table-top steam sterilizers
CSA C22.2 No. 61010-1-12 Safety requirements for electrical equipment for measurement, control and laboratory use, general requirements.
2012/19/EU Waste Electrical and Electronic Equipment (WEEE)
UL 61010-1 Safety requirements for electrical equipment for measurement, control and laboratory use, general requirements.
EN 2014/68/EU Pressure Equipment Directive
The sterilizer can be validated according to EN ISO 17665-1
*On Request
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