E din en iso 8835 2 a1 2009 01 1 1 2009
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E DIN EN ISO 8835-2/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 8835-2/A1:2009-01 Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems.
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E DIN EN ISO 8835-4/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 8835-4/A1:2009-01 Inhalational anaesthesia systems - Part 4: Anaesthetic vapour delivery devices.
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E DIN EN ISO 8835-3/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 8835-3/A1:2009-01 Inhalational anaesthesia systems - Part 3: Transfer and receiving systems of active anaesthetic gas scavenging systems.
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E DIN EN ISO 10651-2/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 10651-2/A1:2009-01 Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 2: Home care ventilators for ventilator-dependent patients.
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E DIN EN 14462/A1:2009-01 1.1.2009
Neplatná norma E DIN EN 14462/A1:2009-01 Surface treatment equipment - Noise test code for surface treatment equipment including its ancillary handling equipment - Accuracy grades 2 and 3.
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E DIN EN ISO 5366-1/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 5366-1/A1:2009-01 Anaesthetic and respiratory equipment - Tracheostomy tubes - Part 1: Tubes and connectors for use in adults.
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E DIN EN ISO 15004-1/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 15004-1/A1:2009-01 Ophthalmic instruments - Fundamental requirements and test methods - Part 1: General requirements applicable to all ophthalmic instruments.
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E DIN EN ISO 13628-1/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 13628-1/A1:2009-01 Petroleum and natural gas industries - Design and operation of subsea production systems - Part 1: General requirements and recommendations - Amendment 1: Revised Clause 6.
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E DIN EN ISO 18778/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 18778/A1:2009-01 Respiratory equipment - Infant monitors - Particular requirements.
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E DIN EN ISO 8359/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 8359/A1:2009-01 Oxygen concentrators for medical use - Safety requirements.
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E DIN EN ISO 7376/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 7376/A1:2009-01 Anaesthetic and respiratory equipment - Laryngoscopes for tracheal intubation.
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E DIN EN ISO 14889/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 14889/A1:2009-01 Ophthalmic optics - Spectacle lenses - Fundamental requirements for uncut finished lenses.
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E DIN EN ISO 12870/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 12870/A1:2009-01 Ophthalmic optics - Spectacle frames - Requirements and test methods.
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E DIN EN ISO 11161/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 11161/A1:2009-01 Safety of machinery - Integrated manufacturing systems - Basic requirements.
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E DIN EN ISO 11979-8/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 11979-8/A1:2009-01 Ophthalmic implants - Intraocular lenses - Part 8: Fundamental requirements.
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E DIN EN ISO 2440/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 2440/A1:2009-01 Flexible and rigid cellular polymeric materials - Accelerated ageing tests - Amendment 1.
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E DIN EN ISO 8185/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 8185/A1:2009-01 Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems.
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E DIN EN ISO 14534/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 14534/A1:2009-01 Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements.
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E DIN EN ISO 14408/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 14408/A1:2009-01 Tracheal tubes designed for laser surgery - Requirements for marking and accompanying information.
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E DIN EN ISO 21647/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 21647/A1:2009-01 Medical electrical equipment - Particular requirements for the basic safety and essential performance of respiratory gas monitors.
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E DIN EN ISO 10651-4/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 10651-4/A1:2009-01 Lung ventilators - Part 4: Particular requirements for operator-powered resuscitators.
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E DIN EN ISO 9919/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 9919/A1:2009-01 Medical electrical equipment - Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use.
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E DIN EN ISO 10651-6/A1:2009-01 1.1.2009
Neplatná norma E DIN EN ISO 10651-6/A1:2009-01 Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6: Home-care ventilatory support devices , English version prEN ISO 10651-6:2008, Amendment 1.
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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 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 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 1756-2/A1:2009-01 1.1.2009
Neplatná norma E DIN EN 1756-2/A1:2009-01 Tail lifts - Platform lifts for mounting on wheeled vehicles - Safety requirements - Part 2: Tail lifts for passengers.
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E DIN EN 378-2/A1:2009-01 1.1.2009
Neplatná norma E DIN EN 378-2/A1:2009-01 Refrigerating systems and heat pumps - Safety and environmental requirements - Part 2: Design, construction, testing, marking and documentation.
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E DIN EN 60320-2-4/A1:2009-01 1.1.2009
Neplatná norma E DIN EN 60320-2-4/A1:2009-01 VDE 0625-2-4/A1. Appliance couplers for household and similar general purposes - Part 2-4: Appliance couplers dependent on appliance weight for engagement.
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E DIN EN 13042-2/A1:2009-01 1.1.2009
Neplatná norma E DIN EN 13042-2/A1:2009-01 Machines and plants for the manufacture, treatment and processing of hollow glass - Safety requirements - Part 2: Handling machines for feeding.
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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 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 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 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 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 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 18369-2/A1:2009-08 1.8.2009
Neplatná norma E DIN EN ISO 18369-2/A1:2009-08 Ophthalmic optics - Contact lenses - Part 2: Tolerances.
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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 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 14155-2/A1:2009-04 1.4.2009
Neplatná norma E DIN EN ISO 14155-2/A1:2009-04 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans.
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E DIN EN ISO 23953-2/A1:2009-09 1.9.2009
Neplatná norma E DIN EN ISO 23953-2/A1:2009-09 Refrigerated display cabinets - Part 2: Classification, requirements and test conditions.
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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 10993-11/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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