NA 176
DIN Standards Committee Health Technologies
DIN ISO 11040-4 [CURRENT] references following documents:
| Document number | Edition | Title |
|---|---|---|
| DIN EN ISO 2039-2 | 2000-01 | Plastics - Determination of hardness - Part 2: Rockwell hardness (ISO 2039-2:1987); German version EN ISO 2039-2:1999 More |
| DIN EN ISO 23908 | 2013-10 | Sharps injury protection - Requirements and test methods - Sharps protection features for single-use hypodermic needles, introducers for catheters and needles used for blood sampling (ISO 23908:2011); German version EN ISO 23908:2013 More |
| DIN EN ISO 527-2 | 2012-06 | Plastics - Determination of tensile properties - Part 2: Test conditions for moulding and extrusion plastics (ISO 527-2:2012); German version EN ISO 527-2:2012 More |
| DIN EN ISO 7864 | 2016-12 | Sterile hypodermic needles for single use - Requirements and test methods (ISO 7864:2016); German version EN ISO 7864:2016 More |
| DIN EN ISO 80369-7 | 2021-08 | Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2021); German version EN ISO 80369-7:2021 More |
| DIN EN ISO 8871-1 | 2004-11 | Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 1: Extractables in aqueous autoclavates (ISO 8871-1:2003); German version EN ISO 8871-1:2004, text in German and English More |
| DIN EN ISO 9626 | 2016-12 | Stainless steel needle tubing for the manufacture of medical devices - Requirements and test methods (ISO 9626:2016); German version EN ISO 9626:2016 More |
| DIN ISO 11040-5 | 2013-12 | Prefilled syringes - Part 5: Plunger stoppers for injectables (ISO 11040-5:2012) More |
| DIN ISO 2859-1 | 2014-08 | Sampling procedures for inspection by attributes - Part 1: Sampling schemes indexed by acceptance quality limit (AQL) for lot-by-lot inspection (ISO 2859-1:1999 + Cor. 1:2001 + Amd.1:2011); Text in German and English More |
| ISO 11137-1 | 2006-04 | Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices More |
