Pelvic organ prolapse surgical mesh, composite-polymer - UK MHRA Medical Device Registration

Pelvic organ prolapse surgical mesh, composite-polymer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 67502. The device is manufactured by JOHNSON & JOHNSON INTERNATIONAL from Belgium, 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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Pelvic organ prolapse surgical mesh, composite-polymer

MHRA Device ID: 67502•Ref: 67502

Device Type

General Medical Device

Devices

Pelvic organ prolapse surgical mesh, composite-polymer

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

May 15, 2024

Manufacturer Information

Name

JOHNSON & JOHNSON INTERNATIONAL

Address

C/O EUROPEAN LOGISTICS CENTRE LEONARDO DA VINCILAAN 15

DIEGEM , Belgium

Created Date

Feb 24, 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 JOHNSON & JOHNSON INTERNATIONAL (10)

Other Products from Same Authorized Representative (10)

Pelvic organ prolapse surgical mesh, composite-polymer - 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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