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

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

For doctor's surgeries

Process validation for washer-disinfectors including Dentsply Sirona DAC Universal and Melag Careclave, manual immersion disinfection, seling 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 washer-disinfectors 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