Wound debridement pad - UK MHRA Medical Device Registration
Wound debridement pad is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122082. The device is manufactured by Coloplast AS from Denmark, classified as General Medical Device. The authorized representative in the UK is Coloplast Ltd.
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Device Type
General Medical Device
Devices
Wound debridement pad
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Mar 15, 2024
Name
Coloplast LtdRelationship Type
Address
Nene Hall Peterborough Business Park
Peterborough, Cambridgeshire, England, United Kingdom
Postcode: PE2 6FX
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