E din en 2438 2009 02 1 2 2009
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E DIN EN 14034-2/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 14034-2/A1:2009-02 Determination of explosion characteristics of dust clouds - Part 2: Determination of the maximum rate of explosion pressure rise (dp/dt)max of dust clouds.
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E DIN EN 71-1/A9:2009-02 1.2.2009
Neplatná norma E DIN EN 71-1/A9:2009-02 Safety of toys - Part 1: Mechanical and physical properties.
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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 13544-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 13544-1/A1:2009-02 Respiratory therapy equipment - Part 1: Nebulizing systems and their components.
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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 61558-2-20:2009-02 1.2.2009
Neplatná norma E DIN EN 61558-2-20:2009-02 VDE 0570-2-20. Safety of transformers, reactors, power supply units and similar products for supply voltages up to 1 100 V - Part 2-20: Particular requirements and tests for small reactors.
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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 60335-1/A101:2009-02 1.2.2009
Neplatná norma E DIN EN 60335-1/A101:2009-02 VDE 0700-1/A76. Household and similar electrical appliances - Safety - Part 1: General requirements.
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E DIN EN 60335-1/A102:2009-02 1.2.2009
Neplatná norma E DIN EN 60335-1/A102:2009-02 VDE 0700-1/A77. Household and similar electrical appliances - Safety - Part 1: General requirements.
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E DIN EN 60335-1/A103:2009-02 1.2.2009
Neplatná norma E DIN EN 60335-1/A103:2009-02 VDE 0700-1/A78. Household and similar electrical appliances - Safety - Part 1: General requirements.
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E DIN EN 60335-1/A104:2009-02 1.2.2009
Neplatná norma E DIN EN 60335-1/A104:2009-02 VDE 0700-1/A79. Household and similar electrical appliances - Safety - Part 1: General requirements.
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E DIN EN 60704-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 60704-1/A1:2009-02 Household and similar electrical appliances - Test code for the determination of airborne acoustical noise - Part 1: General requirements.
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E DIN EN 14492-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 14492-1/A1:2009-02 Cranes - Power driven winches and hoists - Part 1: Power driven winches.
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E DIN EN 1218-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 1218-1/A1:2009-02 Safety of woodworking machines - Tenoning machines - Part 1: Single end tenoning machines with sliding table.
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E DIN EN 1997-1/NA:2009-02 1.2.2009
Neplatná norma E DIN EN 1997-1/NA:2009-02 National Annex - Nationally determined parameters - Eurocode 7: Geotechnical design - Part 1: General rules.
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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 14034-1/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 14034-1/A1:2009-02 Determination of explosion characteristics of dust clouds - Part 1: Determination of the maximum explosion pressure pmax of dust clouds.
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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 13544-3/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 13544-3/A1:2009-02 Respiratory therapy equipment - Part 3: Air entrainment devices.
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E DIN EN 13480-3/A4:2009-02 1.2.2009
Neplatná norma E DIN EN 13480-3/A4:2009-02 Metallic industrial piping - Part 3: Design and calculation.
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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 794-3/A2:2009-02 1.2.2009
Neplatná norma E DIN EN 794-3/A2:2009-02 Lung ventilators - Part 3: Particular requirements for emergency and transport ventilators.
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E DIN EN 61204-7/AA:2009-02 1.2.2009
Neplatná norma E DIN EN 61204-7/AA:2009-02 VDE 0557-7/AA. Low voltage power supplies, d.c. output - Part 7: Safety requirements.
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E DIN EN 12006-3/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 12006-3/A1:2009-02 Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 3: Endovascular devices.
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E DIN EN 1870-12/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 1870-12/A1:2009-02 Safety of woodworking machines - Circular sawing machines - Part 12: Pendulum cross-cut sawing machines.
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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 13035-3/A1:2009-02 1.2.2009
Neplatná norma E DIN EN 13035-3/A1:2009-02 Machines and plants for the manufacture, treatment and processing of flat glass - Safety requirements - Part 3: Cutting machines.
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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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E DIN EN ISO 10993-9/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 10993-9/A1:2009-02 Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products.
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E DIN EN ISO 11140-3/A1:2009-02 1.2.2009
Neplatná norma E DIN EN ISO 11140-3/A1:2009-02 Sterilization of health care products - Chemical indicators - Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test.
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