Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittings; German version EN 1707:1996— 11 стр.
Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (ISO 594-1:1986); German version EN 20594-1:1993— 9 стр.
Injection containers and accessories - Part 1: Injection vials made of glass tubing (ISO 8362-1:2003); German version EN ISO 8362-4:2004, text in German and English— 13 стр.
Injection containers for injectables and accessories - Part 3: Aluminium caps for injection vials (ISO 8362-3:2001); German version EN ISO 8362-3:2003; German and English texts— 18 стр.
Injection containers and accessories - Part 4: Injection vials made of moulded glass (ISO 8362-4:2003); German version EN ISO 8362-4:2004, text in German and English— 17 стр.
Infusion equipment for medical use - Part 2: Closures for infusion bottles (ISO 8536-2:2001); German version EN ISO 8536-2:2002, German and English texts— 19 стр.
Infusion equipment for medical use - Part 2: Closures for infusion bottles (ISO 8536-2:2001), Corrigendum to DIN EN ISO 8536-2:2003-02; German version EN ISO 8536-2:2002/AC:2005— 2 стр.
Infusion equipment for medical use - Part 8: Infusion equipment for use with pressure infusion apparatus (ISO 8536-8:2004); German version EN ISO 8536-8:2004— 16 стр.
Infusion equipment for medical use - Part 9: Fluid lines for use with pressure infusion equipment (ISO 8536-9:2004); German version EN ISO 8536-9:2004— 12 стр.
Infusion equipment for medical use - Part 10: Accessories for fluid lines for use with pressure infusion equipment (ISO 8536-10:2004); German version EN ISO 8536-10:2004— 14 стр.
Infusion equipment for medical use - Part 11: Infusion filters for use with pressure infusion equipment (ISO 8536-11:2004); German version EN ISO 8536-11:2004— 12 стр.
Stainless steel needle tubing for manufacture of medical devices (ISO 9626:1991 + AMD 1:2001) (including amendment A1:2001); German version EN ISO 9626:1995 + A1:2001— 13 стр.
Sterile, single-use intravascular catheters - Part 5: Over-needle peripheral catheters (ISO 10555-5:1996 + AMD 1:2000) (including corrigendum AC:1999 and AMD A1:2000); German version EN ISO 10555-5:1997 + AC:1999 + A1:2000— 16 стр.
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003); German version EN ISO 10993-3:2009— 27 стр.
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002+Amd.1:2006); German version EN ISO 10993-4:2002+A1:2006— 48 стр.
Biological evaluation of medical devices - Part 5: Tests for cytotoxicity: in vitro-methods (ISO 10993-5:1999); German version EN ISO 10993-5:1999— 8 стр.
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007); German version EN ISO 10993-6:2009— 31 стр.
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008); German version EN ISO 10993-7:2008— 108 стр.
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999); German version EN ISO 10993-9:2009— 18 стр.
Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002, including Amd 1:2006); German version EN ISO 10993-10:2009— 68 стр.
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007); German version EN ISO 10993-12:2009— 28 стр.
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998); German version EN ISO 10993-13:2009— 24 стр.
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001); German version EN ISO 10993-14:2009— 23 стр.
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000); German version EN ISO 10993-15:2000— 16 стр.
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997); German version EN ISO 10993-16:2009— 21 стр.
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002); German version EN ISO 10993-17:2009— 38 стр.
Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005); German version EN ISO 10993-18:2009— 28 стр.
Injection containers for injectables and accessories; caps made of aluminium-plastics combinations for injection vials; identical with ISO 8362-6:1992— 5 стр.
Injection containers and accessories - Part 7: Injection caps made of aluminium-plastics combinations without overlapping plastics part (ISO 8362-7:2006)— 10 стр.
Prefilled syringes - Part 4: Glass barrels for injectables and sterilized subassembled syringes ready for filling (ISO 11040-4:2015); Text in German and English— 68 стр.
