CEN/TC 206
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
9478 | LVS EN ISO 10993-11:1995 | Biological evalution of medical devices - Part 11: Tests for systemic toxicity | Atcelts |
9484 | LVS EN ISO 10993-2:2000 | Biological evaluation of medical devices - Part 2: Animal welfare requirements | Atcelts |
32002 | LVS EN ISO 10993-16:2009 | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997) | Atcelts |
32003 | LVS EN ISO 10993-17:2009 | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) | Atcelts |
9496 | LVS EN ISO 10993-4:2003 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | Atcelts |
9486 | LVS EN ISO 10993-12:1996 | Biological evalution of medical devices - Part 12: Sample preparation and reference materials | Atcelts |
9482 | LVS EN ISO 10993-9:2000 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
32766 | LVS EN ISO 10993-12:2012 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) | Atcelts |
9472 | LVS EN 30993-5:1994 | Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992) | Atcelts |
32006 | LVS EN ISO 10993-6:2009 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007) | Atcelts |
Displaying 51-60 of 190 results.