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Last Updated | 25 November 2020 |
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Category: EU Commission
Checklist Instructions For Use for reusable and re‐sterilisable Medical Devices
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Last Updated | 19 August 2020 |
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Fact sheet on MDR requirements for Transparency and Public Information
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Last Updated | 19 August 2020 |
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Unique Device Identification – FAQ
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Last Updated | 11 June 2020 |
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Factsheet for Manufacturers of In-Vitro Diagnostic Medical Devices
Factsheet for Manufacturers of In-Vitro Diagnostic Medical Devices
IVDR, 2017/746/EU Source: http://ec.europa.eu/growth/sectors/medical-devices/ ...
IVDR, 2017/746/EU Source: http://ec.europa.eu/growth/sectors/medical-devices/ ...
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Last Updated | 11 June 2020 |
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Factsheet for Manufacturers of Medical Devices
Factsheet for Manufacturers of Medical Devices
MDR, 2017/745/EU Source: http://ec.europa.eu/growth/sectors/medical-devices/ ...
MDR, 2017/745/EU Source: http://ec.europa.eu/growth/sectors/medical-devices/ ...
Size | 165.40 KB |
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Last Updated | 11 June 2020 |
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Blue Guide: Implementation of EU products rules 2016
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Last Updated | 11 June 2020 |
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