Carbonic bone filling/substitute implant - UK MHRA Medical Device Registration

Carbonic bone filling/substitute implant is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 73261. The device is manufactured by Prosidyan Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson Medical 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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Carbonic bone filling/substitute implant

MHRA Device ID: 73261•Ref: 73261

Device Type

General Medical Device

Devices

Carbonic bone filling/substitute implant

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

May 15, 2024

Manufacturer Information

Name

Prosidyan Inc.

Address

41 Spring St #107

New Providence, United States

Created Date

Apr 14, 2021

Authorized Representative

Name

Johnson & Johnson Medical Ltd

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

DJ Fang

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Other Products from Prosidyan Inc. (1)

Bone grafting cannula

Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Carbonic bone filling/substitute implant - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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