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 159819. The device is manufactured by ZimmerBiomet Spine Inc from United States, classified as General Medical Device. The authorized representative in the UK is Biomet 3i 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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Polymeric spinal interbody fusion cage

MHRA Device ID: 159819•Ref: 159819

Device Type

General Medical Device

Devices

Polymeric spinal interbody fusion cage

Type

Class IIb

Date Registered

Nov 19, 2024

Last Updated

Sep 29, 2023

Manufacturer Information

Name

ZimmerBiomet Spine Inc

Address

10225 Westmoor Drive

Colorado, Westminster, United States

Created Date

Nov 3, 2022

Authorized Representative

Name

Biomet 3i UK Ltd

Relationship Type

UK Responsible Person

Address

1 Glass Wharf Burges Salmon Rep Office

Bristol, England, United Kingdom

Postcode: BS2 0ZX

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Other Products from ZimmerBiomet Spine Inc (10)

Other Products from Same Authorized Representative (10)

Polymeric spinal interbody fusion cage - UK MHRA Medical Device Registration

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Date Registered

Last Updated

Name

Address

Created Date

Name

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DJ Fang

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Metal-polymer composite spinal interbody fusion cage

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