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BSI UK (0086) is a leading full-scope Approved Body under the UK MDR 2002, as amended. We review your medical device to ensure conformity against UK legislation by offering a range of flexible certification services providing you with efficient pathways to bring your product to market.
To understand which requirements you need to meet, you must classify the device and identify the appropriate conformity assessment route for your product. This dictates the required activities to demonstrate conformity.
We will review the route you chose to confirm its suitability, and work with you to execute the most efficient review process for the route selected. Our trusted review processes will allow you to build reliability and confidence into your UKCA marking project planning.
BSI UKAB is designated for all devices covered by UK MDR 2002.
General Medical Devices.
Active Implantable Medical Devices.
In-vitro Diagnostic Medical Devices.
For Northern Ireland, even after 1 July 2025, a CE or UKNI mark will continue to be required for medical devices placed on the NI market and manufacturers will need to meet EU Regulations.
Based on MHRA acceptance of (EU) 2023/607, MDD/AIMDD certified medical devices may be placed on the GB market as follows (only if requirements set out in (EU) 2023/607 are met):
-Class III and IIb implantable non-WET devices till December 2027
-Class IIb WET, Class IIa, Class Im and Is devices till June 2028
We understand the challenges of achieving market access efficiently and safely, meeting commercial goals and regulatory requirements.
Whether you're starting the certification process, looking to transfer or just need to discuss options for your business, we can help.
Discover our experienced and efficient routes to place compliant and safe devices on global markets.
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