Spinal guidewire - UK MHRA Medical Device Registration
Spinal guidewire is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 100102. The device is manufactured by Stryker Spine, a division of Stryker Corporation 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.
Device Type
General Medical Device
Devices
Spinal guidewire
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Dec 5, 2023
Address
2 Pearl Court
Allendale, New Jersey, United States
Created Date
Mar 3, 2021
Name
Stryker UK LtdRelationship Type
Address
Stryker House Hambridge Road
Newbury, Berkshire, England, United Kingdom
Postcode: RG14 5AW
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