Osteotomy guide, reusable - UK MHRA Medical Device Registration
Osteotomy guide, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207352. The device is manufactured by Arthrex Inc. from United States, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class IIa
Status
Date Registered
Dec 18, 2024
Name
Arthrex Inc.Address
1370 Creekside Boulevard
Naples, Florida, United States
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