Bone distraction forceps - UK MHRA Medical Device Registration
Bone distraction forceps is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 186998. 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
Bone distraction forceps
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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