E din en iso 17059 2009 02 1 2 2009
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E DIN EN ISO 17059:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 17059:2009-02 Oilseeds - Extraction of oil and preparation of methyl esters of triglyceride fatty acids for analysis by gas chromatography (Rapid method).
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E DIN EN ISO 7885:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 7885:2009-02 Dentistry - Sterile injection needles for single use.
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E DIN EN ISO 844:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 844:2009-02 Rigid cellular plastics - Determination of compression properties.
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E DIN EN ISO 948:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 948:2009-02 Spices and condiments - Sampling.
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E DIN EN ISO 676:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 676:2009-02 Spices and condiments - Botanical nomenclature.
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E DIN EN ISO 19141:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 19141:2009-02 Geographic information - Schema for moving features.
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E DIN EN ISO 22717:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 22717:2009-02 Cosmetics - Microbiology - Detection of Pseudomonas aeruginosa.
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E DIN EN ISO 22718:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 22718:2009-02 Cosmetics - Microbiology - Detection of Staphylococcus aureus.
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E DIN EN ISO 3218:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 3218:2009-02 Essential oils - Principles of nomenclature.
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E DIN EN ISO 21148:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 21148:2009-02 Cosmetics - Microbiology - General instructions for microbiological examination.
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E DIN EN ISO 21150:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 21150:2009-02 Cosmetics - Microbiology - Detection of Escherichia coli.
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E DIN EN ISO 18416:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 18416:2009-02 Cosmetics - Microbiology - Detection of Candida albicans.
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E DIN EN ISO 845:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 845:2009-02 Cellular plastics and rubbers - Determination of apparent density.
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E DIN EN ISO 939:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 939:2009-02 Spices and condiments - Determination of moisture content - Entrainment method.
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E DIN EN ISO 13720:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 13720:2009-02 Meat and meat products - Enumeration of presumptive Pseudomonas spp..
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E DIN EN ISO 21149:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 21149:2009-02 Cosmetics - Microbiology - Enumeration and detection of aerobic mesophilic bacteria.
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E DIN EN ISO 9920:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 9920:2009-02 Ergonomics of the thermal environment - Estimation of thermal insulation and water vapour resistance of a clothing ensemble.
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E DIN EN ISO 15752:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 15752:2009-02 Ophthalmic instruments - Endoilluminators - Fundamental requirements and test methods for optical radiation safety.
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E DIN EN ISO 25539-2/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 25539-2/A1:2009-02 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents.
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E DIN EN ISO 17072-2:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 17072-2:2009-02 Leather - Chemical determination of metal content - Part 2: Total metal content.
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E DIN EN ISO 11138-2/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 11138-2/A1:2009-02 Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes.
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E DIN EN ISO 5983-2:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 5983-2:2009-02 Animal feeding stuffs - Determination of nitrogen content and calculation of crude protein content - Part 2: Block digestion and steam distillation method.
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E DIN EN ISO 17072-1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 17072-1:2009-02 Leather - Chemical determination of metal content - Part 1: Extractable metals.
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E DIN EN ISO 25539-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 25539-1/A1:2009-02 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses.
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E DIN EN ISO 9360-2/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 9360-2/A1:2009-02 Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml.
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E DIN EN ISO 14855-2:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 14855-2:2009-02 Determination of the ultimate aerobic biodegradability of plastic materials under controlled composting conditions - Method by analysis of evolved carbon dioxide - Part 2: Gravimetric measurement of carbon dioxide evolved in a laboratory-scale test.
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E DIN EN ISO 11140-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 11140-1/A1:2009-02 Sterilization of health care products - Chemical indicators - Part 1: General requirements.
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E DIN EN ISO 10555-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10555-1/A1:2009-02 Sterile, single-use intravascular catheters - Part 1: General requirements.
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E DIN EN ISO 11114-1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 11114-1:2009-02 Transportable gas cylinders - Compatibility of cylinder and valve materials with gas contents - Part 1: Metallic materials.
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E DIN EN ISO 9360-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 9360-1/A1:2009-02 Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml.
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E DIN EN ISO 13982-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 13982-1/A1:2009-02 Protective clothing for use against solid particulates - Part 1: Performance requirements for chemical protective clothing providing protection to the full body against airborne solid particulates (type 5 clothing), Amendment 1.
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E DIN EN ISO 5840/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 5840/A1:2009-02 Cardiovascular implants - Cardiac valve prostheses.
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E DIN EN ISO 16409/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 16409/A1:2009-02 Dentistry - Oral hygiene products - Manual interdental brushes, Amendment 1.
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E DIN EN ISO 24234/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 24234/A1:2009-02 Dentistry - Mercury and alloys for dental amalgam, Amendment 1.
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E DIN EN ISO 5360/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 5360/A1:2009-02 Anaesthetic vaporizers - Agent-specific filling systems.
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E DIN EN ISO 9713/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 9713/A1:2009-02 Neurosurgical implants - Self-closing intracranial aneurysm clips.
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E DIN EN ISO 7197/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 7197/A1:2009-02 Neurosurgical implants - Sterile, single-use hydrocephalus shunts and components.
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E DIN EN ISO 7439/A2:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 7439/A2:2009-02 Copper-bearing intra-uterine contraceptive devices - Requirements, tests.
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E DIN EN ISO 14602/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 14602/A1:2009-02 Non-active surgical implants - Implants for Osteosynthesis - Particular requirements.
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E DIN EN ISO 14607/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 14607/A1:2009-02 Non-active surgical implants - Mammary implants - Particular requirements.
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E DIN EN ISO 14630/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 14630/A1:2009-02 Non-active surgical implants - General requirements.
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E DIN EN ISO 21534/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 21534/A1:2009-02 Non-active surgical implants - Joint replacement implants - Particular requirements.
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E DIN EN ISO 11197/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 11197/A1:2009-02 VDE 0750-211/A1. Medical supply units.
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E DIN EN ISO 22088-5:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 22088-5:2009-02 Plastics - Determination of resistance to environmental stress cracking (ESC) - Part 5: Constant tensile deformation method.
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E DIN EN ISO 22088-6:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 22088-6:2009-02 Plastics - Determination of resistance to environmental stress cracking (ESC) - Part 6: Slow strain rate method.
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E DIN EN ISO 21535/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 21535/A1:2009-02 Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants.
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E DIN EN ISO 21536/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 21536/A1:2009-02 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants.
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E DIN EN ISO 11138-3/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 11138-3/A1:2009-02 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes.
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E DIN EN ISO 10993-10/A2:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-10/A2:2009-02 Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity.
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E DIN EN ISO 10993-11/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-11/A1:2009-02 Biological evaluation of medical devices - Part 11: Tests for systemic toxicity.
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E DIN EN ISO 10993-12/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-12/A1:2009-02 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials.
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E DIN EN ISO 10993-13/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-13/A1:2009-02 Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices.
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E DIN EN ISO 10993-14/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-14/A1:2009-02 Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics.
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E DIN EN ISO 10993-16/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-16/A1:2009-02 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables.
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E DIN EN ISO 10993-17/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-17/A1:2009-02 Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances.
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E DIN EN ISO 10993-18/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-18/A1:2009-02 Biological evaluation of medical devices - Part 18: Chemical characterization of materials.
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E DIN EN ISO 10993-3/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-3/A1:2009-02 Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity.
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E DIN EN ISO 10993-4/A2:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-4/A2:2009-02 Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood.
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E DIN EN ISO 10993-5/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-5/A1:2009-02 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity.
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E DIN EN ISO 10993-6/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-6/A1:2009-02 Biological evaluation of medical devices - Part 6: Tests for local effects after implantation.
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