CEN/TC 206
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
9489 | LVS EN ISO 10993-15:2003 | Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys | Atcelts |
9472 | EN 30993-5:1994 | Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992) | Atcelts |
22132 | EN ISO 10993-2:2006 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) | Atcelts |
9497 | EN ISO 10993-5:1999 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999) | Atcelts |
9486 | EN ISO 10993-12:1996 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:1996) | Atcelts |
27092 | LVS EN ISO 10993-1:2010 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009) | Atcelts |
32766 | EN ISO 10993-12:2012 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) | Atcelts |
9484 | EN ISO 10993-2:1998 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:1992) | Atcelts |
9481 | EN ISO 10993-7:1995 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:1995) | Atcelts |
9480 | EN 30993-6:1994 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:1994) | Atcelts |
Displaying 31-40 of 190 results.