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Bone grafting cannula - UK MHRA Medical Device Registration

Bone grafting cannula is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 73260. 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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General Medical Device
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Bone grafting cannula
MHRA Device ID: 73260โ€ขRef: 73260

Device Type

General Medical Device

Devices

Bone grafting cannula

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

May 15, 2024

Manufacturer Information

Address

41 Spring St #107

New Providence, United States

Created Date

Apr 14, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

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