United Kingdom MHRA device registration 91098

Polyolefin/fluoropolymer suture, monofilament

United Kingdom·General Medical Device·Coloplast Corp·Registered Nov 26, 2024

Registration details

Device ID: 91098
MHRA Reference Number: 91098
Date Registered: Nov 26, 2024
Last Updated: Feb 27, 2024

Device classification

Device Type: General Medical Device
Devices: Polyolefin/fluoropolymer suture, monofilament
Type: Class IIb

Manufacturer

Name: Coloplast Corp
Address: 1601 West River Road
Minneapolis, United States
Created Date: Apr 16, 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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About this record

Polyolefin/fluoropolymer suture, monofilament is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 91098. The device is manufactured by Coloplast Corp from United States, classified as General Medical Device. The authorized representative in the UK is Coloplast Ltd.

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