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About This Item
Full Description
This document specifies the requirements for information supplied by the manufacturer for a medical device or by the manufacturer for an accessory, as defined in 3.1. This document includes the generally applicable requirements for identification and labels on a medical device or accessory, the packaging, marking of a medical device or accessory, and accompanying information. This document does not specify the means by which the information is to be supplied.
All current amendments available at time of purchase are included with the purchase of this document.
Document History
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BS EN ISO 20417:2021
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Medical devices. Information to be supplied by the manufacturer, Incorporating corrigenda May 2021 and May 2022- Most Recent
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BS EN ISO 20417:2021
Medical devices. Information to be supplied by the manufacturer- Historical Version
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BS EN ISO 20417:2021 Draft
Medical devices. Information to be supplied by the manufacturer- Historical Version
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BS EN ISO 20417 Draft
Medical devices. Information to be supplied by the manufacturer- Historical Version
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BS ISO 20417:2021
Medical devices. Information to be supplied by the manufacturer- Historical Version
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BS EN 1041:2008+A1:2013
Information supplied by the manufacturer of medical devices- Historical Version
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BS EN 1041:2008
Information supplied by the manufacturer of medical devices- Historical Version
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BS 06/30123163 DC
BS EN 1041. Information supplied by the manufacturer with medical devices- Historical Version
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BS EN 1041:1998
Information supplied by the manufacturer with medical devices- Historical Version