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 109129. The device is manufactured by Stryker Leibinger GmbH & Co. KG 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.
Device Type
General Medical Device
Devices
Polyethylene craniofacial tissue reconstructive material
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Feb 2, 2024
Address
Botzinger Strasse 41
Freiburg, Germany
Created Date
Mar 26, 2021
Name
Stryker UK LtdRelationship Type
Address
Stryker House Hambridge Road
Newbury, Berkshire, England, United Kingdom
Postcode: RG14 5AW
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