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  2. ISO 13485 - Wikipedia

    en.wikipedia.org/wiki/ISO_13485

    ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.

  3. Device Master Record - Wikipedia

    en.wikipedia.org/wiki/Device_Master_Record

    The sub-clause 4.2.3 of ISO 13485:2016 requires a manufacturer of medical device to establish a Technical file, similar to a device master record. The EU medical device regulation requires a manufacturer of a medical device to maintain a Technical documentation.

  4. Annex SL - Wikipedia

    en.wikipedia.org/wiki/Annex_SL

    The Annex SL is a section of the ISO/IEC Directives part 1 that prescribes how ISO Management System Standard (MSS) standards should be written. The aim of Annex SL is to enhance the consistency and alignment of MSS by providing a unifying and agreed-upon high level structure, identical core text and common terms and core definitions.

  5. Design history file - Wikipedia

    en.wikipedia.org/wiki/Design_history_file

    A design history file is a compilation of documentation that describes the design history of a finished medical device.The design history file, or DHF, is part of regulation introduced in 1990 when the U.S. Congress passed the Safe Medical Devices Act, which established new standards for medical devices that can cause or contribute to the death, serious illness, or injury of a patient.

  6. ISO 9000 family - Wikipedia

    en.wikipedia.org/wiki/ISO_9000_family

    ISO 13485:2016 is the medical industry's equivalent of ISO 9001. ISO 13485:2016 is a stand-alone standard. Because ISO 13485 is relevant to medical device manufacturers (unlike ISO 9001, which is applicable to any industry), and because of the differences between the two standards relating to continual improvement, compliance with ISO 13485 ...

  7. List of ISO standards 12000–13999 - Wikipedia

    en.wikipedia.org/wiki/List_of_ISO_standards_12000...

    ISO 13485:2016 Medical devices – Quality management systems – Requirements for regulatory purposes ISO/IEC 13490 Information technology – Volume and file structure of read-only and write-once compact disk media for information interchange

  8. images.huffingtonpost.com

    images.huffingtonpost.com/2012-08-30-3258_001.pdf

    Created Date: 8/30/2012 4:52:52 PM

  9. List of ISO standards 14000–15999 - Wikipedia

    en.wikipedia.org/wiki/List_of_ISO_standards_14000...

    ISO 14289-1:2014 Part 1: Use of ISO 32000-1 (PDF/UA-1) ISO/TR 14292:2012 Health informatics – Personal health records – Definition, scope and context; ISO 14296:2016 Intelligent transport systems – Extension of map database specifications for applications of cooperative ITS

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