NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 3826-1 [Withdrawn] references following documents:
| Document number | Edition | Title |
|---|---|---|
| ISO 10993-13 | 2010-06 | Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices More |
| ISO 10993-14 | 2001-11 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics More |
| ISO 10993-16 | 2017-05 | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables More |
| ISO 10993-3 | 2014-10 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity More |
| ISO 10993-6 | 2016-12 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation More |
| ISO 10993-7 | 2008-10 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals More |
| ISO 10993-7 Technical Corrigendum 1 | 2009-11 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals; Technical Corrigendum 1 More |
| ISO 15747 | 2018-09 | Plastic containers for intravenous injections More |
| ISO 3826-2 | 2008-08 | Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction leaflets More |
| ISO 3826-3 | 2006-09 | Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features More |
