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GBA MDS - Validation of processing/repeated processing

Validation of processing / repeated processing

Processing/repeated processing of reusable devices (ISO 17664, ANSI AAMI ST81, AAMI TIR12)

  • Worst-case selection
  • Microbiological efficiency control of manual/automated cleaning and disinfection (including procedures for non-critical medical devices)
  • Microbiological efficiency control of sterilization process (steam,…)
  • Protein test in combination with microbiological method
  • TOC test
  • Toxicologically relevant material changes
  • Repeated processing
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If you seek efficient, safe qualification for your processing/reprocessing contact us at

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GBA MDS - Cytotoxicity of medical devices

Cytotoxicity of medical devices

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