Polymeric spinal interbody fusion cage - UK MHRA Medical Device Registration

Polymeric spinal interbody fusion cage is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 97431. The device is manufactured by Depuy Spine Inc. from United States, 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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Polymeric spinal interbody fusion cage

MHRA Device ID: 97431•Ref: 97431

Device Type

General Medical Device

Devices

Polymeric spinal interbody fusion cage

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

May 15, 2024

Manufacturer Information

Name

Depuy Spine Inc.

Address

325 Paramount Drive Paramount Dr Raynham

Bristol, MA, United States

Created Date

Jun 16, 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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Polymeric spinal interbody fusion cage - UK MHRA Medical Device Registration

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DJ Fang

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