Brochure
Medical Devices

General Medical Devices

As a manufacturer of a medical device, you must ensure that you meet the relevant regulatory requirements before placing your product onto the market

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In this brochure:

EU Notified Body and UK Approved Body Expertise
Meet our General Team
From product to market
How BSI supports your market readiness

Insights & Media

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EU MDR – Post Market Clinical Follow-Up

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Annex XVI - Devices Without an Intended Medical Purpose

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Using Standards to Demonstrate Conformity

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Unlocking the Potential of Consumer Wearables in Healthcare

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Medical Device Lifetime - Assisting manufacturers

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Symbols & Details Required for Medical Devices & IVDs

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