Polyethylene craniofacial tissue reconstructive material - UK MHRA Medical Device Registration

Polyethylene craniofacial tissue reconstructive material is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 69490. The device is manufactured by Medtronic Xomed Inc from United States, classified as General Medical Device. The authorized representative in the UK is Medtronic Limited.

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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Polyethylene craniofacial tissue reconstructive material

MHRA Device ID: 69490•Ref: 69490

Device Type

General Medical Device

Devices

Polyethylene craniofacial tissue reconstructive material

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Dec 21, 2023

Manufacturer Information

Name

Medtronic Xomed Inc

Address

6743 Southport Drive North

Jacksonville, FL, United States

Created Date

Mar 15, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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Other Products from Medtronic Xomed Inc (10)

Other Products from Same Authorized Representative (10)

Polyethylene craniofacial tissue reconstructive material - UK MHRA Medical Device Registration

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Devices

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Date Registered

Last Updated

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Address

Created Date

Name

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DJ Fang

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