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 176772. The device is manufactured by TEKNIMED SAS from France, classified as General Medical Device. The authorized representative in the UK is Advena 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: 176772•Ref: 176772

Device Type

General Medical Device

Devices

Bone matrix implant, synthetic, non-antimicrobial

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Mar 7, 2024

Manufacturer Information

Name

TEKNIMED SAS

Address

8 rue du Corps Franc Pommiès

Vic en Bigorre, France

Created Date

Apr 29, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

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Other Products from TEKNIMED SAS (10)

Other Products from Same Authorized Representative (10)

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

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

Radiation therapy software

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