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 131481. The device is manufactured by Naviswiss AG from Switzerland, classified as General Medical Device. The authorized representative in the UK is confinis (UK) RP Ltd.

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Orthopaedic/craniofacial implantation planning software

MHRA Device ID: 131481•Ref: 131481

Device Type

General Medical Device

Devices

Orthopaedic/craniofacial implantation planning software

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Sep 12, 2024

Manufacturer Information

Name

Naviswiss AG

Address

Stahlrain 2 CH-5200

Brugg, Switzerland

Created Date

Jan 7, 2022

Authorized Representative

Name

confinis (UK) RP Ltd

Relationship Type

UK Responsible Person

Address

St John's Innovation Centre Cowley Road

Cambridge, England, United Kingdom

Postcode: CB4 0WS

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Type: General Medical Device

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Orthopaedic/craniofacial implantation planning software - UK MHRA Medical Device Registration

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