Medical Devices

VUOS has long experience with biological evaluation of medical devices. All tests are performed in Quality Assurance System (GLP - Good Laboratory Practice) according to the European Standard EN ISO 10993.

  • Tests for genotoxicity , carcinogenicity and reproductive toxicity: EN ISO 10993-3, EN ISO 10993-2, EN ISO 10993-12
  • Tests for in vitro cytotoxicity: EN ISO 10993-5, EN ISO 10993-12
  • Tests for local effects after implantation: EN ISO 10993-6, EN ISO 10993-2, EN ISO 10993-12
  • Tests for irritation and delayed-type hypersensitivity: EN ISO 10993-10, EN ISO 10993-2, EN ISO 10993-12
  • Tests for systemic toxicity: EN ISO 10993-11, EN ISO 10993-2, EN ISO 10993-12