United Kingdom MHRA device registration 209673

Orthopaedic bone screw (non-sliding)

United Kingdom·System or Procedure Pack·Arthrex Inc.·Registered Jan 28, 2025DREGIY

Registration details

Device ID: 209673
Status: DREGIY
Date Registered: Jan 28, 2025

Device classification

Device Type: System or Procedure Pack
Type: System or Procedure Pack

Manufacturer

Name: Arthrex Inc.
Address: 1370 Creekside Boulevard
Naples, Florida, United States

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About this record

Orthopaedic bone screw (non-sliding) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 209673. The device is manufactured by Arthrex Inc. from United States, classified as System or Procedure Pack.

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