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 72886. The device is manufactured by FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH from Germany, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, 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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Pelvic organ prolapse surgical mesh, synthetic polymer

MHRA Device ID: 72886•Ref: 72886

Device Type

General Medical Device

Devices

Pelvic organ prolapse surgical mesh, synthetic polymer

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH

Address

Prager Ring 70

Aachen , Germany

Created Date

Apr 12, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

DJ Fang

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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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Created Date

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DJ Fang

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