The initial validation that gets your thermal disinfector ready for use.
The standard-compliant initial validation of your washer-disinfector (WD) at commissioning — carried out by certified Steri24 technicians directly at your practice. You receive the documented baseline record that makes your reprocessing audit-proof from day one.
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 need no second point of contact for your WD.
Tecno-Gaz (AquaPlus)AtosMiele
Your model is not listed? No problem — on request we also service devices from other manufacturers. Please enter 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 services
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 waste-water connections as well as correct dosing technology.
Operational Qualification (OQ)
Verification of temperature curves, holding times and sensor technology with calibrated reference probes.
Performance Qualification (PQ)
Evidence of cleaning and disinfection performance with 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 the first contact to the audit-proof protocol — we coordinate everything and come to you.
1
Appointment & preparation
After commissioning, you tell us the device, manufacturer and typical load. We arrange the on-site validation 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 records — 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
Revalidation reminder
We note the next due revalidation for you and get in touch in good time.
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 disruption to your daily practice routine to a minimum.