United Kingdom MHRA device registration 207352
Osteotomy guide, reusable
United Kingdom·General Medical Device·Arthrex Inc.·Registered Dec 18, 2024DREGIYRegistration details
- Device ID
- 207352
- Status
- DREGIY
- Date Registered
- Dec 18, 2024
Device classification
- Device Type
- General Medical Device
- Type
- Class IIa
Manufacturer
- Name
- Arthrex Inc.
- Address
- 1370 Creekside BoulevardNaples, Florida, United States
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About this record
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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