Maintenance + Revalidation Sealing Machine Switzerland

During maintenance, the safety and functionality of the device are thoroughly inspected to ensure safe and reliable operation for the next two years.
If necessary, wear parts such as heating elements or the cutting unit are professionally replaced. In addition, a complete functional test and an electrical safety test are performed.
Maintenance of our sealing machines is required every two years or after 30,000 cycles, in accordance with specifications.

The revalidation of a sealing machine is an essential component of quality assurance in the reprocessing of medical devices. The requirements for process validation are specified in the DIN EN ISO 11607-2 standard and serve to demonstrate a reproducible and safe sealing process. According to the DGSV guidelines and the DIN standard, revalidation should be performed annually or whenever the packaging material is changed.

As part of the validation process, we inspect all relevant process steps of your sealing machine as well as the quality of the resulting seal seams.

Scope of Revalidation

Installation Qualification (IQ)

• User instruction and training, including documentation
• Review of maintenance and calibration schedules

Operational Qualification (OQ)

• Execution of the heat-sealing process in accordance with the manufacturer’s technical data
• Test seals using the recommended limit values
• Sterilization of the prepared samples
• Verification of quality characteristics using:
  • Visual inspection with Seal-Check
  • Seal integrity test
  • Peel test
  • Seal strength testing by an external testing laboratory

Performance Qualification (PQ)

• Determination of the most critical packaging configuration
• Documentation of sterilization batches
• Testing of 3 samples of the same material in different sterilization batches (also possible within a single batch upon agreement)

Seal strength testing in the testing laboratory

Seal strength testing is conducted by an external testing laboratory as part of the validation process. For this purpose, the sealed and sterilized samples are sent to the laboratory and subsequently evaluated. The turnaround time is typically about 10–14 days. Once the laboratory results are available, you will also receive a validation report.