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 73675. 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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Pelvic organ prolapse surgical mesh, synthetic polymer

MHRA Device ID: 73675•Ref: 73675

Device Type

General Medical Device

Devices

Pelvic organ prolapse surgical mesh, synthetic polymer

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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Other Products from Coloplast Corp (3)

Other Products from Same Authorized Representative (10)

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

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

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Address

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