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Medical devices — Information to be supplied by the manufacturer
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Medical devices — Non-electrically driven portable infusion devices
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Medical devices — Part 2: Guidance on the application of usability engineering to medical devices
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Medical devices — Post-market surveillance for manufacturers
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Medical devices — Pump tube spallation test — General procedure
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Medical devices — Quality management systems — Requirements for regulatory purposes
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Medical devices — Sleep apnoea breathing therapy — Masks and application accessories
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Medical devices — Symbols to be used with medical device labels, labelling, and information to be supplied — Part 2: Symbol development, selection and validation
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Medical devices — Transfusion set and blood bag compatibility test method
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Medical devices utilizing animal tissues and their derivatives — Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents
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Medical electrical equipment — Deployment, implementation and operational guidelines for identifying febrile humans using a screening thermograph
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Medical electrical equipment — Part 1-8: General requirements for basic safety and essential performance — Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
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Medical devices — Information to be supplied by the manufacturer

Medical devices — Non-electrically driven portable infusion devices

Medical devices — Part 2: Guidance on the application of usability engineering to medical devices

Medical devices — Post-market surveillance for manufacturers

Medical devices — Pump tube spallation test — General procedure

Medical devices — Quality management systems — Requirements for regulatory purposes

Medical devices — Sleep apnoea breathing therapy — Masks and application accessories

Medical devices — Symbols to be used with medical device labels, labelling, and information to be supplied — Part 2: Symbol development, selection and validation

Medical devices — Transfusion set and blood bag compatibility test method

Medical devices utilizing animal tissues and their derivatives — Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents

Medical electrical equipment — Deployment, implementation and operational guidelines for identifying febrile humans using a screening thermograph

Medical electrical equipment — Part 1-8: General requirements for basic safety and essential performance — Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems

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