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 205917. The device is manufactured by K2M Group Holdings, Inc from United States, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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
Type
Class IIa
Status
Date Registered
Dec 21, 2024
Address
600 Hope Parkway SE
Leesburg, Virginia, United States
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