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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 188172. The device is manufactured by Brainlab Ltd. from Israel, classified as General Medical Device. The authorized representative in the UK is Brainlab 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.

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Orthopaedic/craniofacial implantation planning software
MHRA Device ID: 188172•Ref: 188172

Device Type

General Medical Device

Devices

Orthopaedic/craniofacial implantation planning software

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jun 7, 2024

Manufacturer Information

Address

35 Efal Street

Petah Tikva, Central, Israel

Created Date

Aug 10, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

1010 Cambourne Business Park

Cambridge, England, United Kingdom

Postcode: CB36DP

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