Our hygiene centre.
Safely processed.
Hygienically tested.
The preparation process.
Professional preparation according to MDR specifications.
The cleaning process is carried out in three coordinated steps in separate rooms.
Within this process, we use the special disinfectant Veriforte, which covers a wide spectrum of activity against microorganisms such as bacteria, viruses, fungi and spores. It is applied not only by wiping, but also by fogging or spraying. The product is VAH-approved and all tests are carried out in accordance with RKI guidelines. It dries residue-free and leaves no yellowing on disinfected surfaces.
Services of our hygiene centre.
Reprocessing of bath lifts.
For KANJO bath lifts
- Collection and return shipment
- Professional cleaning and disinfection
- Functional test to ensure operational readiness
- Cost estimation / quote for necessary repairs
- Replacing the suction cups
- Replacing existing seat and backrest covers
- Return shipment in new original packaging including hygiene certificate and user manual
- Function and parts warranty for 12 months
For bath lifts of other manufacturers
- Collection and return shipment
- Professional cleaning and disinfection
- Return shipment with hygiene certificate
Please note:
We do not offer functional tests, repairs or maintenance for products from other manufacturers. The returned products will be cleaned and disinfected before being sent back, without testing or repair.
Quality, testing & certification.
Tested hygiene for maximum safety.
Validated processes, regular inspections and independent certifications ensure the highest standards in reprocessing. Our hygiene centre meets the strictest requirements for quality, safety and traceability.
The seal confirms that a product has been professionally reprocessed using validated procedures in accordance with recognized recommendations (RKI, BfArM, DGKH).
Our quality standards
We work on the basis of clearly defined and legally regulated requirements – always evidence-based and comprehensibly documented.
Validated reprocessing methods based on
- Recommendations of the Robert Koch Institute (RKI)
- Specifications of the Federal Institute for Drugs and Medical Devices (BfArM)
- the guideline of the German Society for Hygiene and Microbiology (DGKM)
Implementation of all relevant legal requirements
- Medical Devices Implementation Act (MPDG)
- Medical Device Operator Ordinance (MPBetreibV)
Internal protection and hygiene concept based on
- of the Infection Protection Act (IfSG)
- the current recommendations of the RKI
- of country-specific guidelines
Certified trust
As a manufacturer of medical devices, the DIETZ GROUP is certified according to the internationally recognized standard DIN EN ISO 13485:2016. In addition, our hygiene center is independently audited annually by PZERT.
In this way, we create transparency and security that you can rely on.
Technical tests
Our medical devices are regularly checked for safety and functionality.
- Safety inspection (STK)
- Functional tests
- Visual inspections
All test results are digitally documented and can be traced at any time.
Hygiene tests during operation
We rely on seamless microbiological monitoring through internal and external tests:
- Bacteria measurement using Lumitest with every cleaning cycle
- Surface checks using impression samples for each cleaning cycle
- Laboratory analysis of all samples by an independent testing institute
In this way, we ensure that our hygiene standards are not only adhered to, but also continuously monitored and optimized.
Preparation of larger quantities
Individual conditions are possible for multiple devices. For further information, please contact our customer service by the form below.
Products & solutions
Support
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