|
DIN EN 1656 |
Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary field - Test method and requirements (phase 2/step 1); English version of DIN EN 1656 |
|
DIN EN 1659 |
In vitro diagnostic systems - Culture media for microbiology: Terminology |
|
DIN EN 1707 |
Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittings |
|
DIN EN 1733 |
Suction catheters for use in the respiratory tract |
|
DIN EN 1820 |
Anaesthetic reservoir bags (ISO 5362:2000, modified) |
|
DIN EN 1826 |
Large-scale process and production in biotechnology - Control procedures for raw materials |
|
DIN EN 1865 |
Specifications for stretchers and other patient handling equipment used in road ambulances |
|
DIN EN 1970 |
Adjustable beds for disabled persons - Requirements and test methods (includes Amendment A1:2005) |
|
DIN EN 1985 |
Walking aids - General requirements and test methods |
|
DIN EN 20594-1 |
Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - General requirements (ISO 594-1:1986) |
|
DIN EN 21942-3 |
Dental vocabulary - Part 3: Dental instruments (ISO 1942-3:1989); German version EN 21942-3:1993 |
|
DIN EN 21942-4 |
Dental vocabulary; dental equipment (ISO 1942-4:1989) |
|
DIN EN 26461-1 |
Water quality; detection and enumeration of the spores of sulfite-reducing anaerobes (clostridia); part 1: method by enrichment in a liquid medium (ISO 6461-1:1986); german version EN 26461-1:1993 |
|
DIN EN 26461-2 |
Water quality; detection and enumeration of the spores of sulfite-reducing anaerobes (clostridia); part 2: method by membrane filtration (ISO 6461-2:1986); german version EN 26461-2:1993 |
|
DIN EN 285 |
Sterilization - Steam sterilizers - Large sterilizers |
|
DIN EN 29168 |
Dental handpieces - Hose connectors (ISO 9168:1991) |
|
DIN EN 30993-6 |
Biological evaluation of medical devices - Tests for local effects after implantation (ISO 10993-6:1994) |
|
DIN EN 375 |
Information supplied by the manufacturer with in vitro diagnostic reagents for professional use; English version of DIN EN 375 |
|
DIN EN 375 |
Information supplied by the manufacturer with in vitro diagnostic reagents for professional use; German version EN 375:2001 |
|
DIN EN 376 |
Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing; German version EN 376:2002, German and English texts |
|
DIN EN 455-1 |
Medical gloves for single use - Part 1: Requirements and testing for freedom from holes; English version of DIN EN 455-1 |
|
DIN EN 475 |
Medical devices - Electrically-generated alarm signals |
|
DIN EN 550 |
Sterilization of medical devices - Validation and routine control of ethylene oxide sterilization |
|
DIN EN 556-1 |
Sterilization of medical devices - Requirements for medical devices to be designated |
|
DIN EN 556-1 Berichtigung 1 |
Sterilization of medical devices - Requirements for medical devices to be designated |
|
DIN EN 556-2 |
Sterilization of medical devices - Requirements for medical devices to be designated STERILE - Part 2: Requirements for aseptically processed medical devices |
|
DIN EN 591 |
Instructions for use for in-vitro-diagnostic instruments for professional use; German version EN 591:2001 |
|
DIN EN 592 |
Instructions for use for in vitro diagnostic instruments for self-testing; German version EN 592:2002; German and English texts |
|
DIN EN 61157 |
(DRAFT) Standard means for the reporting of the acoustic output of medical diagnostic ultrasonic equipment (IEC 87/356/CDV:2006); German version prEN 61157:2006 |
|
DIN EN 62127-1 |
(DRAFT) Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz using hydrophones (IEC 87/352/CDV:2006); German version prEN 62127-1:2006 |
|
DIN EN 62127-2 |
(DRAFT) Ultrasonics - Hydrophones - Part 2: Calibration of hydrophones to be used in ultrasonic fields up to 40 MHz (IEC 87/353/CDV:2006); German version prEN 62127-2:2006 |
|
DIN EN 62127-3 |
(DRAFT) Ultrasonics - Hydrophones - Part 3: Properties of hydrophones for ultrasonic fields up to 40 MHz (IEC 87/354/CDV:2006); German version prEN 62127-3:2006 |
|
DIN EN 737-1 |
Medical gas pipeline systems - Part 1: Terminal units for compressed medical gases and vacuum |
|
DIN EN 737-2 |
Medical gas pipeline systems - Part 2: Anaesthetic gas scavenging disposal systems - Basic requirements (includes Amendment A1:1999); English version DIN EN 737-2:1998 + A1:1999 |
|
DIN EN 737-4 |
Medical gas pipeline systems - Part 4: Terminal units for anaesthetic gas scavenging systems |
|
DIN EN 740 |
Anaesthetic workstations and their modules - Particular requirements (includes Corrigendum AC:1998) |
|
DIN EN 794-1 |
Lung ventilators - Part 1: Particular requirements for critical care ventilators (includes Amendment A1:2000); English version of DIN EN 794-1:1997 + A1:2000 |
|
DIN EN 794-3 |
Lung ventilators - Part 3: Particular requirements for emergency and transport ventilators |
|
DIN EN 794-3/A1 |
Lung ventilators - Part 3: Particular requirements for emergency and transport ventilators |
|
DIN EN 866-4 |
Biological systems for testing sterilizers and sterilization processes - Part 4: Particular systems for use in irradiation sterilizers |
|
DIN EN 866-5 |
Biological systems for testing sterilizers and sterilization processes - Part 5: Particular systems for use in low temperature steam and formaldehyde sterilizers |
|
DIN EN 867-3 |
Non-biological systems for use in sterilizers - Part 3: Specification for Class B indicators for use in the Bowie and Dick test |
|
DIN EN 867-4 |
Non-biological systems for use in sterilizers - Part 4: Specification for indicators as an alternative to the Bowie and Dick test for the detection of steam penetration; English version of DIN EN 867-4 |
|
DIN EN 867-5 |
Non-biological systems for use in sterilizers - Part 5: Specification for indicator systems and process challenge devices for use in performance testing for small sterilizers Type B and Type S; English version of DIN EN 867-5 |
|
DIN EN 868-10 |
Packaging materials and systems for medical devices which are to be sterilized - Part 10: Adhesive coated nonwoven materials of polyolefines for use in the manufacture of heat sealable pouches, reels and lids - Requirements and test methods; English version of DIN EN 868-10 |
|
DIN EN 868-2 |
Packaging materials and systems for medical devices which are to be sterilized - Part 2: Sterilization wrap - Requirements and test methods |
|
DIN EN 868-4 |
Packaging materials and systems for medical devices which are to be sterilized - Part 4: Paper bags - Requirements and test methods |
|
DIN EN 868-5 |
Packaging materials and systems for medical devices which are to be sterilized - Part 5: Heat and self-sealable pouches and reels of paper and plastic film construction; Requirements and test methods (includes Corrigendum AC:2001); English version of DIN EN 868-5:1999 + AC:2001 |
|
DIN EN 868-6 |
Packaging materials and systems for medical devices which are to be sterilized - Part 6: Paper for the manufacture of packs for medical use for sterilization by ethylene oxide or irradiation - Requirements and test methods |
|
DIN EN 868-8 |
Packaging materials and systems for medical devices which are to be sterilized - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods |
|
DIN EN 868-9 |
Packaging materials and systems for medical devices which are to be sterilized - Part 9: Uncoated nonwoven materials of polyolefines for use in the manufacture of heat sealable pouches, reels and lids - Requirements and tests methods; English version of DIN EN 868-9 |
|
DIN EN ISO 10079-1 |
Medical suction equipment - Part 1: Electrically powered suction equipment - Safety requirements (ISO 10079-1:1999); English version of DIN EN ISO 10079-1 |
|
DIN EN ISO 10079-2 |
Medical suction equipment - Part 2: Manually powered suction equipment (ISO 10079-2:1999); English version of DIN EN ISO 10079-2 |
|
DIN EN ISO 10079-3 |
Medical suction equipment - Part 3: Suction equipment powered from a vacuum or pressure source (ISO 10079-3:1999); English version of DIN EN ISO 10079-3 |
|
DIN EN ISO 10139-1 |
Dentistry - Soft lining materials for removable dentures - Part 1: Materials for short-term use (ISO 10139-1:2005) |
|
DIN EN ISO 10139-2 |
Dentistry - Soft lining materials for removable dentures - Part 2: Materials for long-term use (ISO 10139-2:1999); English version of DIN EN ISO 10139-2 |
|
DIN EN ISO 10271 |
Dental metallic materials - Corrosion test methods (ISO 10271:2001); English version of DIN EN ISO 10271 |
|
DIN EN ISO 10271 Berichtigung 1 |
Dental metallic materials - Corrosion test methods (ISO 10271:2001); Corrigendum 1 to English version of DIN EN ISO 10271:2002-01 |
|
DIN EN ISO 10272-1 |
Microbiology of food and animal feeding stuffs - Horizontal method for detection and enumeration of Campylobacter spp. - Part 1: Detection method (ISO 10272-1:2006) |
|
DIN EN ISO 10273 |
Microbiology of food and animal feeding stuffs - Horizontal method for the detection of presumptive pathogenic Yersinia enterocolitica (ISO 10273:2003) |
|
DIN EN ISO 10322-2 |
Ophthalmic optics - Semi-finished spectacle lens blanks - Part 2: Specifications for progressive power lens blanks (ISO 10322-2:2006) |
|
DIN EN ISO 10323 |
Dental rotary instruments - Bore diameters for discs and wheels (ISO 10323:1991) |
|
DIN EN ISO 10328 |
Prosthetics - Structural testing of lower-limb prostheses - Requirements and test methods (ISO 10328:2006) |
|
DIN EN ISO 10341 |
Ophthalmic optics - Refractor heads (ISO 10341:1997) |
|
DIN EN ISO 10342 |
Ophthalmic instruments - Eye refractometers (ISO 10342:2003) |
|
DIN EN ISO 10343 |
Ophthalmic instruments - Ophthalmometers (ISO 10343:1997) |
|
DIN EN ISO 10451 |
Dental implant systems - Contents of technical file (ISO 10451:2002) |
|
DIN EN ISO 10477 |
Dentistry - Polymer-based crown and bridge materials (ISO 10477:2004) |
|
DIN EN ISO 10524-1 |
Pressure regulators for use with medical gases - Part 1: Pressure regulators and pressure regulators with flow-metering devices (ISO 10524-1:2006) |
|
DIN EN ISO 10524-2 |
Pressure regulators for use with medical gases - Part 2: Manifold and line pressure regulators (ISO 10524-2:2005) |
|
DIN EN ISO 10524-3 |
Pressure regulators for use with medical gases - Part 3: Pressure regulators integrated with cylinder valves (ISO 10524-3:2005) |
|
DIN EN ISO 10535 |
Hoists for the transfer of disabled persons - Requirements and test methods (ISO 10535:2006) |
|
DIN EN ISO 10555-2 |
Sterile, single-use intravascular catheters - Part 2: Angiographic catheters (ISO 10555-2:1996) |
|
DIN EN ISO 10555-3 |
Sterile, single-use intravascular catheters - Part 3: Central venous catheters (ISO 10555-3:1996) |
|
DIN EN ISO 10555-4 |
Sterile, single-use intravascular catheters - Part 4: Balloon dilatation catheters (ISO 10555-4:1996) |
|
DIN EN ISO 10555-5 |
Sterile, single-use intravascular catheters - Part 5: Over-needle peripheral catheters (ISO 10555-5:1996 + Amd. 1:2000) (includes Corrigendum AC:1999 and Amendment 1:2000); English version of DIN EN ISO 10555-5:1997 + AC:1999 + A1:2000 |
|
DIN EN ISO 10637 |
Dental equipment - High- and medium-volume suction systems (ISO 10637:1999); English version of DIN EN ISO 10637 |
|
DIN EN ISO 10650-1 |
Dentistry - Powered polymerization activators - Part 1: Quartz tungsten halogen lamps (ISO 10650-1:2004) |
|
DIN EN ISO 10651-2 |
Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 2: Home care ventilators for ventilator-dependent patients (ISO 10651-2:2004) |
|
DIN EN ISO 10651-4 |
Lung ventilators - Part 4: Particular requirements for operator-powered resuscitators (ISO 10651-4:2002) |
|
DIN EN ISO 10651-6 |
Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6: Home-care ventilatory support devices (ISO 10651-6:2004) |
|
DIN EN ISO 10705-1 |
Water quality - Detection and enumeration of bacteriophages - Part 1: Enumeration of F-specific RNA bacteriophages (ISO 10705-1:1995); English version of DIN EN ISO 10705-1 |
|
DIN EN ISO 10705-2 |
Water quality - Detection and enumeration of bacteriophages - Part 2: Enumeration of somatic coliphages (ISO 10705-2:2000); English version of DIN EN ISO 10705-2 |
|
DIN EN ISO 10712 |
Water quality - Pseudomonas putida growth inhibition test (Pseudomonas cell multiplication inhibition test) (ISO 10712:1995) |
|
DIN EN ISO 10938 |
Ophthalmic instruments - Chart projectors (ISO 10938:1998) |
|
DIN EN ISO 10939 |
Ophthalmic instruments - Slit-lamp microscopes (ISO 10939:2007) |
|
DIN EN ISO 10940 |
Ophthalmic instruments - Fundus cameras (ISO 10940:1998); German version EN ISO 10940:1998 |
|
DIN EN ISO 10942 |
Ophthalmic instruments - Direct ophthalmoscopes (ISO 10942:2006) |
|
DIN EN ISO 10943 |
Ophthalmic instruments - Indirect ophthalmoscopes (ISO 10943:2006) |
|
DIN EN ISO 10944 |
Ophthalmic instruments - Synoptophores (ISO 10944:1998); German version EN ISO 10944:1998 |
|
DIN EN ISO 10993-1 |
Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003) |
|
DIN EN ISO 10993-11 |
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006) |
|
DIN EN ISO 10993-12 |
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2002) |
|
DIN EN ISO 10993-13 |
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998) |
|
DIN EN ISO 10993-14 |
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) |
|
DIN EN ISO 10993-15 |
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000); English version of DIN EN ISO 10993-15 |
|
DIN EN ISO 10993-16 |
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997) |
|
DIN EN ISO 10993-17 |
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) |
|
DIN EN ISO 10993-18 |
Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) |
|
DIN EN ISO 10993-2 |
Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) |
|
DIN EN ISO 10993-3 |
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003) |
|
DIN EN ISO 10993-5 |
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999) |
|
DIN EN ISO 10993-7 |
Biological evaluation of medical devices - Ethylene oxide sterilization residuals (ISO 10993-7:1995) |
|
DIN EN ISO 10993-9 |
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999) |
|
DIN EN ISO 11070 |
Sterile single-use intravascular catheter introducers (ISO 11070:1998) |
|
DIN EN ISO 11137-1 |
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006) |
|
DIN EN ISO 11137-3 |
Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006) |
|
DIN EN ISO 11138-1 |
Sterilization of health care products - Biological indicators - Part 1: General requirements (ISO 11138-1:2006) |
|
DIN EN ISO 11138-3 |
Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006) |
|
DIN EN ISO 11138-4 |
Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2006) |
|
DIN EN ISO 11138-5 |
Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes (ISO 11138-5:2006) |
|
DIN EN ISO 11140-1 |
Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2005) |
|
DIN EN ISO 11143 |
Dental equipment - Amalgam separators (ISO 11143:1999 + Cor.1:2002) (includes corrigendum AC:2002) |
|
DIN EN ISO 11144 |
Dental equipment - Connections for supply and waste lines (ISO 11144:1995) |
|
DIN EN ISO 11199-1 |
Walking aids manipulated by both arms - Requirements and test methods - Part 1: Walking frames (ISO 11199-1:1999); English version of DIN EN ISO 11199-1 |
|
DIN EN ISO 11199-2 |
Walking aids manipulated by both arms - Requirements and test methods - Part 2: Rollators (ISO 11199-2:2005) |
|
DIN EN ISO 11199-3 |
Walking aids manipulated by both arms - Requirements and test methods - Part 3: Walking tables (ISO 11199-3:2005) |
|
DIN EN ISO 11244 |
Dental brazing investments (ISO 11244:1998) |
|
DIN EN ISO 11245 |
Dental restorations - Phosphate-bonded refractory die materials (ISO 11245:1999); English version of DIN EN ISO 11245 |
|
DIN EN ISO 11246 |
Dental ethyl silicate bonded casting investments (ISO 11246:1996) |
|
DIN EN ISO 11334-1 |
Assistive products for walking manipulated by one arm - Requirements and test methods - Part 1: Elbow crutches (ISO 11334-1:2007) |
|
DIN EN ISO 11334-4 |
Walking aids manipulated by one arm - Requirements and test methods - Part 4: Walking sticks with three or more legs (ISO 11334-4:1999) |
|
DIN EN ISO 1135-4 |
Transfusion equipment for medical use - Part 4: Transfusion sets for single use (ISO 1135-4:2004) |
|
DIN EN ISO 11380 |
Ophthalmic optics - Formers (ISO 11 380:1994) |
|
DIN EN ISO 11381 |
Ophthalmic optics - Screw threads for use with spectacle frames (ISO 11 381:1994) |
|
DIN EN ISO 11498 |
Dental handpieces - Dental low-voltage electrical motors (ISO 11498:1997) |
|
DIN EN ISO 11499 |
Dental cartridges for local anaesthetics (ISO 11499:1997) |
|
DIN EN ISO 11607-1 |
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006) |
|
DIN EN ISO 11607-2 |
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006) |
|
DIN EN ISO 11608-1 |
Pen-injectors for medical use - Part 1: Pen-injectors; Requirements and test methods (ISO 11608-1:2000); English version of DIN EN ISO 11608-1 |
|
DIN EN ISO 11608-2 |
Pen-injectors for medical use - Part 2: Needles; Requirements and test methods (ISO 11608-2:2000); English version of DIN EN ISO 11608-2 |
|
DIN EN ISO 11608-3 |
Pen-injectors for medical use - Part 3: Finished cartridges; Requirements and test methods (ISO 11608-3:2000); English version of DIN EN ISO 11608-3 |
|
DIN EN ISO 11683 |
Tactile warnings of danger on packaging - Requirements (ISO 11683:1997) |
|
DIN EN ISO 11721-1 |
Determination of resistance of cellulose-containing textiles to micro-organisms - Soil burial test - Part 1: Assessment of rot-retardant finishing (ISO 11721-1:2001); English version of DIN EN ISO 11721-1 |
|
DIN EN ISO 11721-2 |
Textiles - Determination of the resistance of cellulose containing textiles to micro-organisms; Soil burial test - Part 2: Identification of long-term resistance of a rot retardant finish (ISO 11721-2:2003) |
|
DIN EN ISO 11733 |
Water quality - Determination of the elimination and biodegradability of organic compounds in an aqueous medium - Activated sludge simulation test (ISO 11733:2004) |
|
DIN EN ISO 11737-1 |
Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006) |
|
DIN EN ISO 11737-2 |
Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization process (ISO 11737-2:1998); English version of DIN EN ISO 11737-2 |
|
DIN EN ISO 11810-1 |
Lasers and laser-related equipment - Test method and classification for the laser resistance of surgical drapes and/or patient protective covers - Part 1: Primary ignition and penetration (ISO 11810-1:2005) |
|
DIN EN ISO 11978 |
Contact lenses and contact lens care products - Information supplied by the manufacturer (ISO 11978:2000); English version of DIN EN ISO 11978 |
|
DIN EN ISO 11979-1 |
Ophthalmic implants - Intraocular lenses - Part 1: Vocabulary (ISO 11979-1:2006) |
|
DIN EN ISO 11979-10 |
Ophthalmic implants - Intraocular lenses - Part 10: Phakic intraocular lenses (ISO 11979-10:2006) |
|
DIN EN ISO 11979-2 |
Ophthalmic implants - Intraocular lenses - Part 2: Optical properties and test methods (ISO 11979-2:1999); English version of DIN EN ISO 11979-2 |
|
DIN EN ISO 11979-2 Berichtigung 1 |
Ophthalmic implants - Intraocular lenses - Optical properties and test methods (ISO 11979-2:1999); Corrigenda to DIN EN ISO 11979-2:2000-07 |
|
DIN EN ISO 11979-3 |
Ophthalmic implants - Intraocular lenses - Part 3: Mechanical properties and test methods (ISO 11979-3:2006) |
|
DIN EN ISO 11979-4 |
Ophthalmic implants - Intraocular lenses - Part 4: Labelling and information (ISO 11979-4:2000); English version of DIN EN ISO 11979-4 |
|
DIN EN ISO 11979-5 |
Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility (ISO 11979-5:2006) |
|
DIN EN ISO 11979-7 |
Ophthalmic implants - Intraocular lenses - Part 7: Clinical investigations (ISO 11979-7:2006) |
|
DIN EN ISO 11979-8 |
Ophthalmic implants - Intraocular lenses - Part 8: Fundamental requirements (ISO 11979-8:2006) |
|
DIN EN ISO 11979-9 |
Ophthalmic implants - Intraocular lenses - Part 9: Multifocal intraocular lenses (ISO 11979-9:2006) |
|
DIN EN ISO 11981 |
Contact lenses and contact lens care products - Determination of physical compatibility of contact lens care products with contact lenses (ISO 11981:1999) |
|
DIN EN ISO 11985 |
Contact lenses - Ageing by exposure to UV and visible radiation (in vitro method) (ISO 11985:1997) |
|
DIN EN ISO 11986 |
Contact lenses and contact lens care products - Guidelines for the determination of preservative uptake and release (ISO 11986:1999); English version of DIN EN ISO 11986 |
|
DIN EN ISO 11987 |
Contact lenses - Determination of shelf-life (ISO 11987:1997) |
|
DIN EN ISO 11990 |
Optics and optical instruments - Lasers and laser-related equipment - Determination of laser resistance of tracheal tube shafts (ISO 11990:2003) |
|
DIN EN ISO 12864 |
Contact lenses - Determination of scattered light (ISO 12864:1997) |
|
DIN EN ISO 12865 |
Ophthalmic instruments - Retinoscopes (ISO 12865:2006) |
|
DIN EN ISO 12867 |
Ophthalmic instruments - Trial frames (ISO 12867:1998) |
|
DIN EN ISO 12870 |
Ophthalmic optics - Spectacle frames - Requirements and test methods (ISO 12870:2004) |
|
DIN EN ISO 13212 |
Contact lense care products - Guidelines for determination of shelf-life (ISO 13212:1999) |
|
DIN EN ISO 13230 |
Ophthalmic optics - Bar code specifications (ISO 13230:1990) |
|
DIN EN ISO 13294 |
Dental handpieces - Dental air-motors (ISO 13294:1997) |
|
DIN EN ISO 13295 |
Dental rotary instruments - Mandrels (ISO 13295:1994) |
|
DIN EN ISO 13366-1 |
Enumeration of somatic cells in milk - Part 1: Microscopic method (ISO 13366-1:1997) |
|
DIN EN ISO 13366-2 |
Enumeration of somatic cells in milk - Part 2: Electronic particle counter method (ISO 13366-2:1997) |
|
DIN EN ISO 13366-3 |
Enumeration of somatic cells in milk - Part 3: Fluoro-opto-electronic method (ISO 13366-3:1997) |
|
DIN EN ISO 13397-1 |
Peridontal curettes, dental scalers and excavators - General requirements (ISO 13397-1:1995) |
|
DIN EN ISO 13397-2 |
Dentistry - Periodontal curettes, dental scalers and excavators - Part 2: Periodontal curettes of Gr-type (ISO 13397-2:2005) |
|
DIN EN ISO 13397-3 |
Periodontal curettes, dental scalers and excavators - Part 3:H-type dental scalers (ISO 13397-3:1996) |
|
DIN EN ISO 13397-4 |
Periodontal curettes, dental scalers and excavators - Part 4: Dental excavators, discoid type (ISO 13397-4:1997) |
|
DIN EN ISO 13402 |
Surgical and dental hand instruments - Determination of resistance against autoclaving, corrosion and thermal exposure (ISO 13402:1995); English version of DIN EN ISO 13402 |
|
DIN EN ISO 13485 |
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) |
|
DIN EN ISO 13666 |
Ophthalmic optics - Spectacle lenses - Vocabulary (ISO 13666:1998); German version EN ISO 13666:1998 |
|
DIN EN ISO 13716 |
Dentistry - Reversible-irreversible hydrocolloid impression material systems (ISO 13716:1999); English version of DIN EN ISO 13716 |
|
DIN EN ISO 13897 |
Dentistry - Amalgam capsules (ISO 13897:2003) |
|
DIN EN ISO 13969 |
Milk and milk products - Guidelines for a standardized description of microbial inhibitor tests (ISO 13969:2003) |
|
DIN EN ISO 14155-1 |
Clinical investigation of medical devices for human subjects - Part 1: General requirements (ISO 14155-1:2003) |
|
DIN EN ISO 14160 |
Sterilization of single-use medical devices incorporating materials of animal origin - Validation and routine control of sterilization by liquid chemical sterilants (ISO 14160:1998); German version EN ISO 14160:1998 |
|
DIN EN ISO 14161 |
Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results (ISO 14161:2000); English version of DIN EN ISO 14161 |
|
DIN EN ISO 14233 |
Dentistry - Polymer-based die materials (ISO 14233:2003) |
|
DIN EN ISO 14356 |
Dentistry - Duplicating material (ISO 14356:2003) |
|
DIN EN ISO 14408 |
Tracheal tubes designed for laser surgery - Requirements for marking and accompanying information (ISO 14408:2005) |
|
DIN EN ISO 14534 |
Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements (ISO 14534:2002) |
|
DIN EN ISO 14602 |
Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:1998) |
|
DIN EN ISO 14607 |
Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2007) |
|
DIN EN ISO 14630 |
Non-active surgical implants - General requirements (ISO 14630:2005) |
|
DIN EN ISO 14729 |
Contact lens care products - Microbiological requirements and test methods for products and regimens for hygienic management of contact lenses (ISO 14729:2001); English version of DIN EN ISO 14729 |
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DIN EN ISO 14730 |
Contact lens care products - Antimicrobial preservative efficacy testing and guidance on determining discard date (ISO 14730:2000); English version of DIN EN ISO 14730 |
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DIN EN ISO 14801 |
Dentistry - Fatigue test for endosseous dental implants (ISO 14801:2003) |
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DIN EN ISO 14889 |
Ophthalmic optics - Spectacle lenses - Fundamental requirements for uncut finished lenses (ISO 14889:2003) |
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DIN EN ISO 14937 |
General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2000); English version of DIN EN ISO 14937 |
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DIN EN ISO 14971 |
Medical devices - Application of risk management to medical devices (ISO 14971:2000); English version of DIN EN ISO 14971 |
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DIN EN ISO 14971/A1 |
Medical devices - Application of risk management to medical devices - Amendment 1: Rationale for requirements (ISO 14971:2000/AMD 1:2003) |
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DIN EN ISO 15001 |
Anaesthetic and respiratory equipment - Compatibility with oxygen (ISO 15001:2003) |
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DIN EN ISO 15004-1 |
Ophthalmic instruments - Fundamental requirements and test methods - Part 1: General requirements applicable to all ophthalmic instruments (ISO 15004-1:2006) |
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DIN EN ISO 15087-1 |
Dental elevators - Part 1: General requirements (ISO 15087-1:1999); English version of DIN EN ISO 15087-1 |
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DIN EN ISO 15087-2 |
Dental elevators - Part 2: Warwick James elevators (ISO 15087-2:2000); English version of DIN EN ISO 15087-2 |
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DIN EN ISO 15087-3 |
Dental elevators - Part 3: Cryer elevators (ISO 15087-3:2000); English version of DIN EN ISO 15087-3 |
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DIN EN ISO 15087-4 |
Dental elevators - Part 4: Coupland elevators (ISO 15087-4:2000); English version of DIN EN ISO 15087-4 |
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DIN EN ISO 15087-5 |
Dental elevators - Part 5: Bein elevators (ISO 15087-5:2000); English version of DIN EN ISO 15087-5 |
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DIN EN ISO 15087-6 |
Dental elevators - Part 6: Flohr elevators (ISO 15087-6:2000); English version of DIN EN ISO 15087-6 |
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DIN EN ISO 15098-1 |
Dental tweezers - Part 1: General requirements (ISO 15098-1:1999); English version of DIN EN ISO 15098-1 |
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DIN EN ISO 15098-2 |
Dental tweezers - Part 2: Meriam types (ISO 15098-2:2000); English version of DIN EN ISO 15098-2 |
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DIN EN ISO 15098-3 |
Dental tweezers - Part 3: College types (ISO 15098-3:2000); English version of DIN EN ISO 15098-3 |
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DIN EN ISO 15189 |
Medical laboratories - Particular requirements for quality and competence (ISO 15189:2003) |
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DIN EN ISO 15195 |
Laboratory medicine - Requirements for reference measurement laboratories (ISO 15195:2003) |
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DIN EN ISO 15197 |
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003); German version EN ISO 15197:2003, text German and English |
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DIN EN ISO 15225 |
Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange (ISO 15225:2000 + Amd 1:2004) |
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DIN EN ISO 15253 |
Ophthalmic optics and instruments - Optical devices for enhancing low-vision (ISO 15253:2000); English version of DIN EN ISO 15253 |
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DIN EN ISO 15254 |
Ophthalmic optics and instruments - Electro-optical devices for enhancing low vision (ISO 15254:2002) |
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DIN EN ISO 1562 |
Dentistry - Casting gold alloys (ISO 1562:2004) |
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DIN EN ISO 1564 |
Dental aqueous impression materials based on agar (ISO 1564:1995) |
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DIN EN ISO 1567 |
Dentistry - Denture base polymers (ISO 1567:1999); English version of DIN EN ISO 1567 |
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DIN EN ISO 15798 |
Ophthalmic implants - Ophthalmic viscosurgical devices (ISO 15798:2001); English version of DIN EN ISO 15798 |
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DIN EN ISO 15798 Berichtigung 1 |
Ophthalmic implants - Ophthalmic viscosurgical devices (ISO 15798:2001); Corrigenda to DIN EN ISO 15798:2001-12 |
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DIN EN ISO 15841 |
Dentistry - Wires for use in orthodontics (ISO 15841:2006) |
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DIN EN ISO 15854 |
Dentistry - Casting and baseplate waxes (ISO 15854:2005) |
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DIN EN ISO 15882 |
Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of results (ISO 15882:2003) |
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DIN EN ISO 15883-1 |
Washer-disinfectors - Part 1: General requirements, terms and definitions and tests (ISO 15883-1:2006) |
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DIN EN ISO 15883-2 |
Washer-disinfectors - Part 2: Requirements and tests for washer-disinfectors employing thermal disinfection for surgical instruments, anaesthetic equipment, bowls, dishes, receivers, utensiles, glassware, etc. (ISO 15883-2:2006) |
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DIN EN ISO 15883-3 |
Washer-disinfectors - Part 3: Requirements and tests for washer-disinfectors employing thermal disinfection for human waste containers (ISO 15883-3:2006) |
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DIN EN ISO 15912 |
Dentistry - Casting investments and refractory die materials (ISO 15912:2006) |
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DIN EN ISO 16021 |
Urine-absorbing aids - Basic principles for evaluation of single-use adult-incontinence-absorbing aids from the perspective of users and caregivers (ISO 16021:2000); English version of DIN EN ISO 16021 |
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DIN EN ISO 16140 |
Microbiology of food and animal feeding stuffs - Protocol for the validation of alternative methods (ISO 16140:2003) |
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DIN EN ISO 16201 |
Technical aids for persons with disability - Environmental control systems for daily living (ISO 16201:2006) |
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DIN EN ISO 16284 |
Ophthalmic optics - Information interchange for ophthalmic optical equipment (ISO 16284:2006) |
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DIN EN ISO 16408 |
Dentistry - Oral hygiene products - Oral rinses (ISO 16408:2004) |
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DIN EN ISO 16654 |
Microbiology of food and animal feeding stuffs - Horizontal method for the detection of Escherichia coli O157 (ISO 16654:2001); English version of EN ISO 16654:2001:2001 |
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DIN EN ISO 16671 |
Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO 16671:2003) |
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DIN EN ISO 16672 |
Ophthalmic implants - Ocular endotamponades (ISO 16672:2003) |
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DIN EN ISO 16744 |
Dentistry - Base metal materials for fixed dental restorations (ISO 16744:2003) |
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DIN EN ISO 17510-2 |
Sleep apnoea breathing therapy - Part 2: Masks and application accessories (ISO 17510-2:2003) |
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DIN EN ISO 17511 |
In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials (ISO 17511:2003) |
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DIN EN ISO 17664 |
Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004) |
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DIN EN ISO 17665-1 |
Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006) |
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DIN EN ISO 1797-2 |
Dental rotary instruments - Shanks made of plastics (ISO 1797-2:1992) |
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DIN EN ISO 17994 |
Water quality - Criteria for establishing equivalence between microbiological methods (ISO 17994:2004) |
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DIN EN ISO 18153 |
In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003) |
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DIN EN ISO 18369-1 |
Ophthalmic optics - Contact lenses - Part 1: Vocabulary, classification system and recommendations for labelling specifications (ISO 18369-1:2006) |
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DIN EN ISO 18369-2 |
Ophthalmic optics - Contact lenses - Part 2: Tolerances (ISO 18369-2:2006) |
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DIN EN ISO 18369-3 |
Ophthalmic optics - Contact lenses - Part 3: Measurement methods (ISO 18369-3:2006) |
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DIN EN ISO 18369-4 |
Ophthalmic optics - Contact lenses - Part 4: Physicochemical properties of contact lens materials (ISO 18369-4:2006) |
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DIN EN ISO 18777 |
Transportable liquid oxygen systems for medical use - Particular requirements (ISO 18777:2005) |
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DIN EN ISO 18778 |
Respiratory equipment - Infant monitors - Particular requirements (ISO 18778:2005) |
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DIN EN ISO 18779 |
Medical devices for conserving oxygen and oxygen mixtures - Particular requirements (ISO 18779:2005) |
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DIN EN ISO 19054 |
Rail systems for supporting medical equipment (ISO 19054:2005) |
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DIN EN ISO 1942-5 |
Dental vocabulary - Terms associated with testing (ISO 1942-5:1989) |
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DIN EN ISO 19458 |
Water quality - Sampling for microbiological analysis (ISO 19458:2006) |
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DIN EN ISO 19980 |
Ophthalmic instruments - Corneal topographers (ISO 19980:2005) |
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DIN EN ISO 20776-1 |
Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2006) |
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DIN EN ISO 20837 |
Microbiology of food and animal feeding stuffs - Polymerase chain reaction (PCR) for the detection of food-borne pathogens - Requirements for sample preparation for qualitative detection (ISO 20837:2006) |
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DIN EN ISO 20838 |
Microbiology of food and animal feeding stuffs - Polymerase chain reaction (PCR) for the detection of food-borne pathogens - Requirements for amplification and detection for qualitative methods (ISO 20838:2006) |
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DIN EN ISO 21171 |
Medical gloves - Determination of removable surface powder (ISO 21171:2006) |
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DIN EN ISO 21187 |
Milk - Quantitative determination of bacteriological quality - Guidance for establishing and verifying a conversion relationship between routine method results and anchor method results (ISO 21187:2004) |
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DIN EN ISO 21530 |
Dentistry - Materials used for dental equipment surfaces - Determination of resistance to chemical disinfectants (ISO 21530:2004) |
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DIN EN ISO 21533 |
Dentistry - Reusable cartridge syringes intended for intraligamentary injections (ISO 21533:2003) |
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DIN EN ISO 21567 |
Microbiology of food and animal feeding stuffs - Horizontal method for the detection of Shigella spp. (ISO 21567:2004) |
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DIN EN ISO 2157 |
Dental rotary instruments - Nominal diameters and designation code number (ISO 2157:1992) |
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DIN EN ISO 21649 |
Needle-free injectors for medical use - Requirements and test methods (ISO 21649:2006) |
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DIN EN ISO 21671 |
Dentistry - Rotary polishers (ISO 21671:2006) |
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DIN EN ISO 21871 |
Microbiology of food and animal feeding stuffs - Horizontal method for the determination of low numbers of presumptive Bacillus cereus - Most probable number technique and detection method (ISO 21871:2006) |
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DIN EN ISO 21969 |
High-pressure flexible connections for use with medical gas systems (ISO 21969:2005) |
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DIN EN ISO 22112 |
Dentistry - Artificial teeth for dental prostheses (ISO 22112:2005) |
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DIN EN ISO 22174 |
Microbiology of food and animal feeding stuffs - Polymerase chain reaction (PCR) for the detection of food-borne pathogens - General requirements and definitions (ISO 22174:2005) |
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DIN EN ISO 22523 |
External limb prostheses and external orthoses - Requirements and test methods (ISO 22523:2006) |
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DIN EN ISO 22610 |
Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Test method to determine the resistance to wet bacterial penetration (ISO 22610:2006) |
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DIN EN ISO 22612 |
Clothing for protection against infectious agents - Test method for resistance to dry microbial penetration (ISO 22612:2005) |
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DIN EN ISO 22674 |
Dentistry - Metallic materials for fixed and removable restorations and appliances (ISO 22674:2006) |
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DIN EN ISO 22675 |
Prosthetics - Testing of ankle-foot devices and foot units - Requirements and test methods (ISO 22675:2006) |
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DIN EN ISO 22803 |
Dentistry - Membrane materials for guided tissue regeneration in oral and maxillofacial surgery - Contents of a technical file (ISO 22803:2004) |
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DIN EN ISO 22870 |
Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006) |
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DIN EN ISO 24234 |
Dentistry - Mercury and alloys for dental amalgam (ISO 24234:2004) |
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DIN EN ISO 3107 |
Dentistry - Zinc oxide/eugenol and zinc oxide/non-eugenol cements (ISO 3107:2004) |
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DIN EN ISO 3107 Berichtigung 1 |
Dentistry - Zinc oxide/eugenol and zinc oxide/non-eugenol cements (ISO 3107:2004); Corrigendum 1 to English version of DIN EN ISO 3107:2005-01 |
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DIN EN ISO 3630-2 |
Dental root-canal instruments - Part 2: Enlargers (ISO 3630-2:2000); English version of DIN EN ISO 3630-2 |
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DIN EN ISO 3630-3 |
Dental root-canal instruments - Condensers, pluggers and spreaders (ISO 3630-3:1994) |
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DIN EN ISO 3823-1 |
Dental rotary instruments - Burs - Part 1: Steel and carbide burs (ISO 3823-1:1997) |
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DIN EN ISO 3823-2 |
Dentistry - Rotary bur instruments - Part 2: Finishing burs (ISO 3823-2:2003) |
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DIN EN ISO 3826-1 |
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2003) |
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DIN EN ISO 3950 |
Dentistry - Designation system for teeth and areas of the oral cavity (ISO 3950:1984 + Corr:1995) |
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DIN EN ISO 4049 |
Dentistry - Polymer-based filling, restorative and luting materials (ISO 4049:2000); English version of DIN EN ISO 4049 |
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DIN EN ISO 407 |
Small medical gas cylinders - Pin-index yoke-type valve connections (ISO 407:2004) |
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DIN EN ISO 4073 |
Dental equipment - Items of dental equipment at the working place - Identification system (ISO 4073:1980) |
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DIN EN ISO 4074 |
Natural latex condoms - Requirements and test methods (ISO 4074:2002) |
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DIN EN ISO 4135 |
Anaesthetic and respiratory equipment - Vocabulary (ISO 4135:2001); Trilingual version EN ISO 4135:2001 |
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DIN EN ISO 4823 |
Dentistry - Elastomeric impression materials (ISO 4823:2000); English version of DIN EN ISO 4823 |
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DIN EN ISO 4833 |
Microbiology of food and animal feeding stuffs - Horizontal method for the enumeration of microorganisms - Colony-count technique at 30 °C (ISO 4833:2003) |
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DIN EN ISO 5356-1 |
Anaesthetic and respiratory equipment - Conical connectors - Part 1: Cones and sockets (ISO 5356-1:2004) |
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DIN EN ISO 5366-1 |
Anaesthetic and respiratory equipment - Tracheostomy tubes - Part 1: Tubes and connectors for use in adults (ISO 5366-1:2000) |
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DIN EN ISO 5840 |
Cardiovascular implants - Cardiac valve prostheses (ISO 5840:2005) |
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DIN EN ISO 595-2 |
Reusable all-glass or metal-and-glass syringes for medical use - design, performance requirements and tests (ISO 595-2:1987) |
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DIN EN ISO 6009 |
Hypodermic needles for single use - Colour coding for identification (ISO 6009:1992) |
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DIN EN ISO 6222 |
Water quality - Enumeration of culturable micro-organisms - Colony count by inoculation in a nutrient agar culture medium (ISO 6222:1999) |
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DIN EN ISO 6360-2 |
Dentistry - Number coding system for rotary instruments - Part 2: Shapes (ISO 6360-2:2004) |
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DIN EN ISO 6360-3 |
Dentistry - Number coding system for rotary instruments - Part 3: Specific characteristics of burs and cutters (ISO 6360-3:2005) |
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DIN EN ISO 6360-4 |
Dentistry - Number coding system for rotary instruments - Part 4: Specific characteristics of diamond instruments (ISO 6360-4:2004) |
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DIN EN ISO 6360-6 |
Dentistry - Number coding system for rotary instruments - Part 6: Specific characteristics of abrasive instruments (ISO 6360-6:2004) |
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DIN EN ISO 6360-7 |
Dentistry - Number coding system for rotary instruments - Part 7: Specific characteristics of mandrels and special instruments (ISO 6360-7:2006) |
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DIN EN ISO 6871-1 |
Dental base metal casting alloys - Part 1: Cobalt-based alloys (ISO 6871-1:1994) |
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DIN EN ISO 6871-2 |
Dental base metal casting alloys - Part 2: Nickel-based alloys (ISO 6871-2:1994) |