Polyolefin/fluoropolymer suture, monofilament - UK MHRA Medical Device Registration

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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Polyolefin/fluoropolymer suture, monofilament

MHRA Device ID: 91098•Ref: 91098

Device Type

General Medical Device

Devices

Polyolefin/fluoropolymer suture, monofilament

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Feb 27, 2024

Manufacturer Information

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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Polyolefin/fluoropolymer suture, monofilament - UK MHRA Medical Device Registration

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