ProVal - your partner for the validation of reprocessing processes in your reprocessing unit for medical devices

We validate your entire reprocessing chain using all standard procedures. Our highly trained service team collaborates closely with our accredited laboratory to ensure a smooth, efficient process, from sampling and measurement to the validation report. ProVal offers process validation and requalification for washer-disinfectors, sterilizers, container and trolley washers, sealing devices, and endoscope storage cabinets.

For doctor's surgeries

We validate the process for washer-disinfectors, including the Dentsply Sirona DAC Universal and the Melag CareClave. We also validate manual immersion disinfection, sealing devices, and steam sterilizers according to DIN EN 13060 and DIN EN 285.

For central sterilizations (CSSD´s)

Process validation for:

Manual immersion disinfection
Washer-disinfectors, including those for endoscopes
Container and trolley washers
Sealing devices
Drying cabinets
Steam and VH₂O₂ sterilizers

Out services for your CSSD/RUMED:

We support you with comprehensive expertise in the validation and performance qualification of all reprocessing processes in your facility: field-tested and customised. Our service portfolio includes

Validation of automated cleaning and disinfection processes in accordance with DIN EN ISO 15883

Validation of container washing systems in accordance with DIN EN ISO 15883
Validation of steam sterilisation processes in accordance with DIN EN ISO 17665, DIN EN 285 and DIN EN 13060
Validation of the Dentsply Sirona DAC Universal according to DIN EN 13060 and DIN EN ISO 15883
Validation of the Melag Careclave in accordance with DIN EN 13060 and DIN EN ISO 15883
Validation of packaging processes in accordance with DIN EN ISO 11607-2 and the DGSV validation guideline
Validation of the reprocessing of flexible endoscopes in accordance with DIN EN ISO 15883-4
Validation of endoscope storage cabinets with drying function