Orthopaedic guidewire, reusable - UK MHRA Medical Device Registration

Orthopaedic guidewire, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99417. The device is manufactured by Stryker Trauma GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Stryker UK Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, 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.

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Orthopaedic guidewire, reusable

MHRA Device ID: 99417•Ref: 99417

Device Type

General Medical Device

Devices

Orthopaedic guidewire, reusable

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 22, 2023

Manufacturer Information

Name

Stryker Trauma GmbH

Address

Professor-Kuntschnerstrasse 1

Schonkirchen, Germany

Created Date

Mar 17, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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Other Products from Stryker Trauma GmbH (10)

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Orthopaedic guidewire, reusable - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Created Date

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