United Kingdom MHRA device registration 207547

Metal-polymer composite spinal interbody fusion cage

United Kingdom·General Medical Device·Aesculap AG·Registered Dec 20, 2024DREGIY

Registration details

Device ID: 207547
Status: DREGIY
Date Registered: Dec 20, 2024

Device classification

Device Type: General Medical Device
Type: Class III

Manufacturer

Name: Aesculap AG
Address: Am Aesculap Platz
Tuttlingen, Germany

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About this record

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.

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