CEN/TC 206
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
9475 | LVS EN 30993-3:1993 | Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
27092 | EN ISO 10993-1:2009 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO/FDIS 10993-1:2009) | Atcelts |
32007 | EN ISO 10993-11:2009 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) | Atcelts |
77933 | prEN ISO 10993-11 | Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2025) | Aptauja slēgta |
78988 | prEN ISO 10993-3 | Biological evaluation of medical devices - Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity (ISO/DIS 10993-3:2025) | Aptauja slēgta |
60721 | EN ISO 10993-1:2020 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10) | Standarts spēkā |
68925 | LVS EN ISO 10993-23:2021 | Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021) | Standarts spēkā |
60724 | LVS EN ISO 10993-16:2018 | Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017) | Standarts spēkā |
65481 | LVS EN ISO 22442-2:2021 | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020) | Standarts spēkā |
65481 | EN ISO 22442-2:2020 | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020) | Standarts spēkā |
Displaying 131-140 of 190 results.