Peristomal/periwound dressing - UK MHRA Medical Device Registration

Peristomal/periwound dressing is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122212. 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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Peristomal/periwound dressing

MHRA Device ID: 122212•Ref: 122212

Device Type

General Medical Device

Devices

Peristomal/periwound dressing

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Mar 15, 2024

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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Peristomal/periwound dressing - UK MHRA Medical Device Registration

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Date Registered

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Created Date

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