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.
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Device Type
General Medical Device
Type
Class III
Status
Date Registered
Dec 20, 2024
Name
Aesculap AGAddress
Am Aesculap Platz
Tuttlingen, Germany
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