United Kingdom MHRA device registration 207398

Bone matrix implant, synthetic, non-antimicrobial

United Kingdom·General Medical Device·curasan AG·Registered Dec 21, 2024DREGIY

Registration details

Device ID: 207398
Status: DREGIY
Date Registered: Dec 21, 2024

Device classification

Device Type: General Medical Device
Type: Class III

Manufacturer

Name: curasan AG
Address: Lindigstrasse 4
Kleinostheim, Germany

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About this record

Bone matrix implant, synthetic, non-antimicrobial is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207398. The device is manufactured by curasan AG from Germany, classified as General Medical Device.

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