Orthopaedic guidewire, single-use - UK MHRA Medical Device Registration
Orthopaedic guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 212346. The device is manufactured by Biomet Orthopaedics from United States, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class I
Status
Date Registered
Mar 6, 2025
Address
56 East Bell Drive, P.O. Box 587
Warsaw, Indiana , United States
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Manufacturer: Orthofix S.r.l.
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Manufacturer: Orthofix S.r.l.
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