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Processing

GBA MDS - Validation of processing/repeated processing

Validation of processing / repeated processing

Processing/repeated processing of reusable devices (ISO 17664-1/2, AAMI TIR12, ANSI AAMI ST98)

  • Worst-case selection
  • Microbiological efficiency control of manual/automated cleaning and disinfection (including procedures for non-critical medical devices) by high-sensitive microbiological method, protein test or TOC test
  • Microbiological efficiency control of sterilization process (steam,…)
  • Simulation of single and repeated processing
  • Toxicologically relevant material changes
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Ready to take your medical devices to the next level? Contact us today to learn how our comprehensive MedTech solutions can support your needs.

Email: medical-devices@gba-group.com

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