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 64589. The device is manufactured by ETHICON LLC from United States, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson Medical Ltd.

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Pelvic organ prolapse surgical mesh, synthetic polymer

MHRA Device ID: 64589•Ref: 64589

Device Type

General Medical Device

Devices

Pelvic organ prolapse surgical mesh, synthetic polymer

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

May 15, 2024

Manufacturer Information

Name

ETHICON LLC

Address

HIGHWAY 183 KM 8.3

SAN LORENZO, PUERTO RICO, United States

Created Date

Jan 22, 2021

Authorized Representative

Name

Johnson & Johnson Medical Ltd

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

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Other Products from ETHICON LLC (10)

Other Products from Same Authorized Representative (10)

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

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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