General internal orthopaedic fixation system implantation kit - UK MHRA Medical Device Registration
General internal orthopaedic fixation system implantation kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 127332. The device is manufactured by Orthofix S.r.l. from Italy, classified as System or Procedure Pack. The authorized representative in the UK is Emergo Consulting (UK) Limited .
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
System or Procedure Pack
Devices
General internal orthopaedic fixation system implantation kit
Type
System or Procedure Pack
Last Updated
Oct 13, 2022
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 โ UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
General internal orthopaedic fixation system implantation kit
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
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General internal orthopaedic fixation system implantation kit
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General internal orthopaedic fixation system implantation kit
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
General internal orthopaedic fixation system implantation kit
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
General internal orthopaedic fixation system implantation kit
Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
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Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
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Type: System or Procedure Pack
Manufacturer: Orthofix S.r.l.
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Manufacturer: Orthofix S.r.l.
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Type: General Medical Device
Manufacturer: Orthofix S.r.l.

