Bone-screw internal spinal fixation system, sterile - UK MHRA Medical Device Registration

Bone-screw internal spinal fixation system, sterile is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 75476. The device is manufactured by joimax GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, 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.

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Bone-screw internal spinal fixation system, sterile

MHRA Device ID: 75476•Ref: 75476

Device Type

General Medical Device

Devices

Bone-screw internal spinal fixation system, sterile

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

joimax GmbH

Address

Amalienbadstr. 41 RaumFabrik 61

Karlsruhe, Baden Württemberg, Germany

Created Date

Apr 23, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Bone-screw internal spinal fixation system, sterile - UK MHRA Medical Device Registration

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Date Registered

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