Bone file/rasp, manual, reusable - UK MHRA Medical Device Registration
Bone file/rasp, manual, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 197364. The device is manufactured by K2M Group Holdings, Inc 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
Bone file/rasp, manual, reusable
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Jan 30, 2024
Address
600 Hope Parkway SE
Leesburg, Virginia, United States
Created Date
Mar 17, 2021
Name
Stryker UK LtdRelationship Type
Address
Stryker House Hambridge Road
Newbury, Berkshire, England, United Kingdom
Postcode: RG14 5AW
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