Metal-polymer composite spinal interbody fusion cage - UK MHRA Medical Device Registration

Metal-polymer composite spinal interbody fusion cage is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207547. The device is manufactured by Aesculap AG from Germany, classified as General Medical Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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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General Medical Device

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Metal-polymer composite spinal interbody fusion cage

MHRA Device ID: 207547

Device Type

General Medical Device

Type

Class III

Status

DREGIY

Date Registered

Dec 20, 2024

Manufacturer Information

Name

Aesculap AG

Address

Am Aesculap Platz

Tuttlingen, Germany

DJ Fang

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Metal-polymer composite spinal interbody fusion cage - UK MHRA Medical Device Registration

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Date Registered

Name

Address

DJ Fang

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