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 78120. The device is manufactured by Centinel Spine LLC from United States, classified as General Medical Device. The authorized representative in the UK is QARA Business Solutions Ltd.

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Polymeric spinal interbody fusion cage

MHRA Device ID: 78120•Ref: 78120

Device Type

General Medical Device

Devices

Polymeric spinal interbody fusion cage

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Apr 13, 2024

Manufacturer Information

Name

Centinel Spine LLC

Address

900 Airport Road Suite 3B West Chester Pennsylvania 19380 USA

West Chester, United States

Created Date

Apr 25, 2021

Authorized Representative

Name

QARA Business Solutions Ltd

Relationship Type

UK Responsible Person

Address

Coverdale House 10, Purshall Close Redditch

Redditch, Worcestershire, United Kingdom

Postcode: B974PD

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Polymeric spinal interbody fusion cage - UK MHRA Medical Device Registration

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Created Date

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Relationship Type

Address

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Polymeric spinal interbody fusion cage