Bone file/rasp, manual, reusable - UK MHRA Medical Device Registration
Bone file/rasp, manual, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 131755. The device is manufactured by Arthrex Inc from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .
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Device Type
General Medical Device
Devices
Bone file/rasp, manual, reusable
Type
Class IIa
Date Registered
Sep 22, 2021
Last Updated
Dec 22, 2022
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 – UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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