Revalidation that keeps your thermal disinfector standard-compliant.
The recurring revalidation of your washer-disinfector (WD) — usually annually. Our certified technicians confirm on site that your device continues to reliably maintain the validated condition, and provide the complete documentation for it.
Switzerland
To EN ISO 15883 Manufacturer-independent On site in Switzerland
Manufacturer-independent
We validate thermal disinfectors from all manufacturers.
No matter which manufacturer your device comes from — our certified technicians validate it professionally. You don’t need a second point of contact for your WD.
Tecno-Gaz (AquaPlus)AtosMiele
Your model isn’t listed? No problem — on request we also service devices from other manufacturers. Please state the model of your thermal disinfector in the comment field of your order.
Legal certainty
Why validation is mandatory in Switzerland
Requirements in Switzerland
SN EN ISO 15883 · Swissmedic
SN EN ISO 15883: normative basis for WD processes.
Swissmedic & SGSV guideline: validation and routine monitoring of reprocessing.
Operator obligation for annual revalidation of the reprocessing processes.
Documented release of every validated batch.
Technically sound: Thermal disinfection typically takes place at 90–95 °C. For the safe reprocessing of surgical instruments, an A₀ value of 3000 (equivalent to 90 °C for 5 minutes) is the benchmark.
Scope of service
What our validation delivers
Three qualification stages to EN ISO 15883 — fully documented and audit-proof.
Installation Qualification (IQ)
Inspection of installation, water, power and wastewater connections as well as the correct dosing technology.
Operational Qualification (OQ)
Verification of temperature curves, holding times and sensor technology with calibrated reference probes.
Performance Qualification (PQ)
Proof of cleaning and disinfection performance with practice-realistic load patterns and soiling control (A₀ value).
Validation report & label
Complete, standard-compliant documentation to present during inspections — plus a test label on the device.
Process
How your appointment works
From first contact to the audit-proof protocol — we coordinate everything and come to you.
1
Appointment & preparation
You tell us the device, manufacturer and load pattern. We arrange a suitable revalidation appointment.
Phone · Form
2
IQ & OQ on site
The technician checks the installation and operating parameters with calibrated measuring equipment — without bringing your operation to a standstill.
On site
3
Performance qualification
Several measurement cycles with real load patterns, temperature probes and soiling control.
EN ISO 15883
4
Evaluation & report
You receive the complete validation report with all measurement protocols — archivable in an audit-proof manner.
Documentation
5
Release & label
If the test is passed, we mark your device with a test label including the due date.
Release
6
Reminder for the next revalidation
We get in touch in good time before the next due revalidation — you won’t miss a deadline.
Service
On site & personal
No shipping. No downtime.
Your thermal disinfector stays where it is — our technician comes to you directly in Switzerland with calibrated measuring equipment. This keeps your reprocessing ready for use and the interference with day-to-day practice minimal.