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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MHRA Registered

General Medical Device

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Osteotomy guide, reusable

MHRA Device ID: 207352

Device Type

General Medical Device

Type

Class IIa

Status

DREGIY

Date Registered

Dec 18, 2024

Manufacturer Information

Name

Arthrex Inc.

Address

1370 Creekside Boulevard

Naples, Florida, United States

DJ Fang

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Osteotomy guide, reusable - UK MHRA Medical Device Registration

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