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 210396. The device is manufactured by Biomet Orthopaedics from United States, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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
Type
Class IIa
Status
Date Registered
Feb 13, 2025
Address
56 East Bell Drive, P.O. Box 587
Warsaw, Indiana , United States
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Orthopaedic guidewire, single-use
Type: General Medical Device
Registered: Mar 6, 2025
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