Orthopaedic/craniofacial implantation planning software - UK MHRA Medical Device Registration
Orthopaedic/craniofacial implantation planning software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 183370. The device is manufactured by Peek Health, S.A. from Portugal, classified as General Medical Device. The authorized representative in the UK is CASUS UKRP LTD.
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Device Type
General Medical Device
Devices
Orthopaedic/craniofacial implantation planning software
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Nov 5, 2024
Address
Centro de Negócios Ideia Atlântico Rua Padres Carmelitas
Braga, Portugal
Created Date
Dec 18, 2023
Name
CASUS UKRP LTDRelationship Type
Address
107-111 Fleet Street
London, England, United Kingdom
Postcode: EC4A 2AB
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