Custom-made orthopaedic/craniofacial surgical guide - UK MHRA Medical Device Registration

Custom-made orthopaedic/craniofacial surgical guide is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 134631. The device is manufactured by Wright Medical Technology, Inc. from United States, 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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Custom-made orthopaedic/craniofacial surgical guide

MHRA Device ID: 134631•Ref: 134631

Device Type

General Medical Device

Devices

Custom-made orthopaedic/craniofacial surgical guide

Type

Custom-made - Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 31, 2024

Manufacturer Information

Name

Wright Medical Technology, Inc.

Address

1023 Cherry Rd

Memphis, Tennessee, United States

Created Date

Apr 26, 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 Wright Medical Technology, Inc. (10)

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Custom-made orthopaedic/craniofacial surgical guide - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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