External orthopaedic fixation system, single-use - UK MHRA Medical Device Registration
External orthopaedic fixation system, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 185899. The device is manufactured by Orthofix S.r.l. from Italy, classified as General Medical Device. The authorized representative in the UK is CASUS UKRP 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
External orthopaedic fixation system, single-use
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
May 4, 2024
Name
CASUS UKRP LTDRelationship Type
Address
107-111 Fleet Street
London, England, United Kingdom
Postcode: EC4A 2AB
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External orthopaedic fixation system, reusable
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External orthopaedic fixation system, reusable
Type: General Medical Device
External orthopaedic fixation system, single-use
Type: General Medical Device
External orthopaedic fixation system, single-use
Type: System or Procedure Pack
External orthopaedic fixation system, single-use
Type: General Medical Device
External orthopaedic fixation system, single-use
Type: General Medical Device
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