Lumboperitoneal shunt - UK MHRA Medical Device Registration

Lumboperitoneal shunt is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 76651. The device is manufactured by Integra LifeSciences Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Integra Neurosciences 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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Lumboperitoneal shunt

MHRA Device ID: 76651•Ref: 76651

Device Type

General Medical Device

Devices

Lumboperitoneal shunt

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

May 1, 2024

Manufacturer Information

Name

Integra LifeSciences Corporation

Address

1100 Campus Road

Princeton, United States

Created Date

Apr 27, 2021

Authorized Representative

Name

Integra Neurosciences Limited

Relationship Type

UK Responsible Person

Address

Regus Rourke House, Office #113 Watermans Business Park The Causeway

Staines, England, United Kingdom

Postcode: TW18 3BA

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Other Products from Integra LifeSciences Corporation (10)

Other Products from Same Authorized Representative (10)

Lumboperitoneal shunt - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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