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

Bone-screw internal spinal fixation system connector is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 202130. The device is manufactured by SYNTHES GMBH from Switzerland, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson Medical 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 connector

MHRA Device ID: 202130•Ref: 202130

Device Type

General Medical Device

Devices

Bone-screw internal spinal fixation system connector

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Aug 10, 2024

Manufacturer Information

Name

SYNTHES GMBH

Address

EIMATTSTRASSE 3

4436 OBERDORF, Switzerland

Created Date

Feb 21, 2021

Authorized Representative

Name

Johnson & Johnson Medical Ltd

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

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

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