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 78389. The device is manufactured by Stryker Spine, a division of Stryker Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Stryker 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: 78389•Ref: 78389

Device Type

General Medical Device

Devices

Polymeric spinal interbody fusion cage

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Dec 5, 2023

Manufacturer Information

Name

Stryker Spine, a division of Stryker Corporation

Address

2 Pearl Court

Allendale, New Jersey, United States

Created Date

Mar 3, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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Polymeric spinal interbody fusion cage - UK MHRA Medical Device Registration

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Devices

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Date Registered

Last Updated

Name

Address

Created Date

Name

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DJ Fang

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