Features
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COMMUNICATION.
The VeriDoc 2C system features a USB interface for exporting process data to a USB flash drive or external hard drive. This enables electronic documentation, complete traceability and statistical analysis without requiring an additional computer.
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ValiPrint – LABEL PRINTER.
Combined with hawo Duplex indicator labels, the ValiPrint label printer ensures packaging labelling in accordance with current RKI recommendations. The printer housing features an antibacterial coating, while the control panel incorporates a tested antibacterial material.
The following label versions are available:
- Steam (STEAM)
- Steam / Ethylene Oxide (STEAM/ETO)
- Steam / Formaldehyde (STEAM/FORM)
- Plasma (VH₂O₂)
VeriDoc 2C can optionally be equipped with a second ValiPrint label printer, allowing two different sterilization processes (e.g. Steam and Plasma) to be handled within one system. -
INTEGRATION.
Whether using sealable pouches and reels, sterilization wrap or reusable sterilization containers, VeriDoc 2C supports healthcare professionals in complying with the packaging identification requirements of the current RKI recommendations—from sterilization monitoring using an integrated process indicator through to release for storage and documentation in the patient record.
Following the mandatory visual inspection of the sterile barrier system, the operator confirms whether the package has passed or failed the inspection. According to the result, the system automatically prints a label stating either "Sterile Barrier System Approved" or "Sterile Barrier System Not Approved". Packages that fail the inspection must not be used.
All required information — including batch number, operator identification, product description and expiry date — is captured using the easy-to-operate ValiScan 2D barcode scanner together with an individually configured Data Matrix code list and transferred directly to the PrintBox for label printing.
The integrated Class 1 process indicator according to ISO 11140-1 provides visual confirmation that the packaged instrument or set has been processed in a sterilization cycle. After sterilization, the designated approval field allows personalized release for storage.
Following treatment or surgery, the labels can be attached directly to the patient record, providing documented evidence that every instrument or set has been correctly packaged, sterilized and released.
Alternatively, the approval field can be replaced by a QR code containing all relevant package information, enabling fast and reliable transfer into electronic documentation and traceability systems.
