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Directive 98/79/EC - Medical devices: in vitro diagnostic (Back to full list)
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Info on European Standards
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Electrical equipment in medical practice
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In vitro diagnostic medical devices
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Industrial-process measurement, control and automation
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Quality management and corresponding general aspects for medical devices
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Safety of measuring, control, and laboratory equipment
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Sterilization of medical devices
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System aspects
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Disclaimer:
This information is of a general nature and is not a legal advice.
Neither the European Commission, EFTA, CEN, CENELEC, ETSI nor any person acting on behalf of these Institutions/Organisations is responsible for the use which might be made of the information.
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