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 80019. The device is manufactured by MEDOS INTERNATIONAL SARL from Switzerland, 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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Bone grafting cannula

MHRA Device ID: 80019•Ref: 80019

Device Type

General Medical Device

Devices

Bone grafting cannula

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

May 15, 2024

Manufacturer Information

Name

MEDOS INTERNATIONAL SARL

Address

CHEMIN-BLANC 38

LE LOCLE, Switzerland

Created Date

Apr 21, 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

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Other Products from MEDOS INTERNATIONAL SARL (10)

Other Products from Same Authorized Representative (10)

Bone grafting cannula - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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