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 73001. The device is manufactured by Boston Scientific Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Boston Scientific Limited.

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: 73001•Ref: 73001

Device Type

General Medical Device

Devices

Pelvic organ prolapse surgical mesh, synthetic polymer

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 18, 2024

Manufacturer Information

Name

Boston Scientific Corporation

Address

300 Boston Scientific Way

Marlborough, Massachusetts, United States

Created Date

Apr 13, 2021

Authorized Representative

Name

Boston Scientific Limited

Relationship Type

UK Responsible Person

Address

Breakspear Park Breakspear Way

Hemel Hempstead, Hertfordshire, England, United Kingdom

Postcode: HP2 4TZ

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

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Date Registered

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Created Date

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