Biological evaluation of medical devices - Tests for in vitro cytotoxicity Ingestion-build-64721 BS EN 10311 applies to

BS EN 10311 applies to joints for use with non-alloy steel tubular products for use with all types of aqueous liquids

but also on the design

conditioning of test pieces

La PAS 99:2006 è stata progettata per aiutare le organizzazioni nell'integrazione dei sistemi di gestione: l'obiettivo è applicare i requisiti comuni in modo più semplice ed efficace

Description of data fields and entering rules

Biological evaluation of medical devices - Tests for in vitro cytotoxicity Ingestion-build-64721 BS EN 10311 applies toBS EN ISO 10993 5: 2009 Biological evaluation of medical devices. Tests for in vitro cytotoxicity (ISO 10993 5: 2009) BS EN ISO 10993 5 has been revised and now contains informative annexes that identify the sections of the standard that conform to the Medical Devices Directives 93 42 EEC and 90 385 EEC, for medical devices and active implantable medical devices. BS EN ISO 10993 1 is part of the ISO 10993 series that consists of the following parts,