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

Pelvic organ prolapse surgical mesh, synthetic polymer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 163408. The device is manufactured by Coloplast AS from Denmark, classified as General Medical Device. The authorized representative in the UK is Coloplast 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, synthetic polymer

MHRA Device ID: 163408•Ref: 163408

Device Type

General Medical Device

Devices

Pelvic organ prolapse surgical mesh, synthetic polymer

Type

Class III

Date Registered

Apr 23, 2021

Last Updated

Mar 11, 2023

Manufacturer Information

Name

Coloplast AS

Address

Holtedam 1

Humlebaek, Denmark

Created Date

Apr 23, 2021

Authorized Representative

Name

Coloplast Ltd

Relationship Type

UK Responsible Person

Address

Nene Hall Peterborough Business Park

Peterborough, Cambridgeshire, England, United Kingdom

Postcode: PE2 6FX

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

Device Type

Devices

Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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Pelvic organ prolapse surgical mesh, synthetic polymer

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