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 120528. The device is manufactured by Biomet Sports Medicine from United States, classified as General Medical Device. The authorized representative in the UK is Zimmer Biomet UK Limited.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Device Type
General Medical Device
Devices
Bone file/rasp, manual, reusable
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Apr 23, 2024
Address
56 East Bell Drive
Warsaw, Indiana, United States
Created Date
Apr 26, 2021
Relationship Type
Address
Stella Building Windmill Hill Business Park Whitehill Way
Swindon, England, United Kingdom
Postcode: SN5 6NX
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Registered: Nov 26, 2024
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Type: General Medical Device
Manufacturer: Biomet Orthopaedics
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Type: General Medical Device
Manufacturer: Biomet Orthopaedics
Acetabulum prosthesis hole plug
Type: General Medical Device
Manufacturer: Biomet Orthopaedics
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Type: General Medical Device
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