CEN/TC 205
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 9415 | LVS ENV 12719:2002 | Medical thrombosis prophylaxis hosiery | Atcelts |
| 9315 | LVS ENV 12718:2002 | Medical compression hosiery | Atcelts |
| 38135 | LVS EN ISO 9626:2016 | Stainless steel needle tubing for the manufacture of medical devices - Requirements and test methods (ISO 9626:2016) | Standarts spēkā |
| 9442 | LVS EN ISO 9626:2003/A1:2016 | Stainless steel needle tubing for the manufacture of medical devices (ISO 9626:1991/AM 1:2001) | Atcelts |
| 9393 | LVS EN ISO 9626:2003 +A1 | Stainless steel needle tubing for the manufacture of medical devices | Atcelts |
| 76900 | LVS EN ISO 8871-5:2025 | Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2025) | Standarts spēkā |
| 60187 | LVS EN ISO 8871-5:2017 | Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2016) | Atcelts |
| 40957 | LVS EN ISO 8871-5:2014 | Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2005) | Atcelts |
| 21462 | LVS EN ISO 8871-4:2006 | Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 4: Biological requirements and test methods | Standarts spēkā |
| 66886 | LVS EN ISO 8871-3:2004/A1:2019 | Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count - Amendment 1 (ISO 8871-3:2003/Amd 1:2018) | Standarts spēkā |
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