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 67206. The device is manufactured by SYNTHES GMBH from Switzerland, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson Medical 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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Polyethylene craniofacial tissue reconstructive material

MHRA Device ID: 67206•Ref: 67206

Device Type

General Medical Device

Devices

Polyethylene craniofacial tissue reconstructive material

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Aug 10, 2024

Manufacturer Information

Name

SYNTHES GMBH

Address

EIMATTSTRASSE 3

4436 OBERDORF, Switzerland

Created Date

Feb 21, 2021

Authorized Representative

Name

Johnson & Johnson Medical Ltd

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

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Other Products from SYNTHES GMBH (10)

Other Products from Same Authorized Representative (10)

Polyethylene craniofacial tissue reconstructive material - UK MHRA Medical Device Registration

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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