Bone matrix implant, synthetic, non-antimicrobial - UK MHRA Medical Device Registration

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 68967. The device is manufactured by curasan AG from Germany, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, Ltd. .

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, 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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Bone matrix implant, synthetic, non-antimicrobial

MHRA Device ID: 68967•Ref: 68967

Device Type

General Medical Device

Devices

Bone matrix implant, synthetic, non-antimicrobial

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

curasan AG

Address

Lindigstrasse 4

Kleinostheim, Germany

Created Date

Mar 9, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Bone matrix implant, synthetic, non-antimicrobial - UK MHRA Medical Device Registration

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Date Registered

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Created Date

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