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 157046. The device is manufactured by KLS Martin SE & Co. KG from Germany, classified as General Medical Device. The authorized representative in the UK is confinis (UK) RP 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: 157046•Ref: 157046

Device Type

General Medical Device

Devices

Polyethylene craniofacial tissue reconstructive material

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Nov 6, 2024

Manufacturer Information

Name

KLS Martin SE & Co. KG

Address

KLS Martin Platz 1

Tuttlingen, Germany

Created Date

Sep 30, 2022

Authorized Representative

Name

confinis (UK) RP Ltd

Relationship Type

UK Responsible Person

Address

St John's Innovation Centre Cowley Road

Cambridge, England, United Kingdom

Postcode: CB4 0WS

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Other Products from KLS Martin SE & Co. KG (10)

Other Products from Same Authorized Representative (10)

Polyethylene craniofacial tissue reconstructive material - 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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