Custom-made orthopaedic/craniofacial surgical guide - UK MHRA Medical Device Registration

Custom-made orthopaedic/craniofacial surgical guide is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 192739. The device is manufactured by OSSIS Corporation from New Zealand, classified as General Medical Device. The authorized representative in the UK is Zimmer Biomet 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.

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Custom-made orthopaedic/craniofacial surgical guide

MHRA Device ID: 192739•Ref: 192739

Device Type

General Medical Device

Devices

Custom-made orthopaedic/craniofacial surgical guide

Type

Custom-made

Date Registered

Nov 26, 2024

Last Updated

May 10, 2024

Manufacturer Information

Name

OSSIS Corporation

Address

Unit 7 / 2 Barry Hogan Place

Christchurch, Riccarton, New Zealand

Created Date

May 7, 2024

Authorized Representative

Name

Zimmer Biomet UK Limited

Relationship Type

UK Responsible Person

Address

Stella Building Windmill Hill Business Park Whitehill Way

Swindon, England, United Kingdom

Postcode: SN5 6NX

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Other Products from OSSIS Corporation (3)

Other Products from Same Authorized Representative (10)

Custom-made orthopaedic/craniofacial surgical guide - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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