Ventriculoperitoneal shunt - UK MHRA Medical Device Registration

Ventriculoperitoneal shunt is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 76643. 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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Ventriculoperitoneal shunt

MHRA Device ID: 76643•Ref: 76643

Device Type

General Medical Device

Devices

Ventriculoperitoneal 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)

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Ventriculoperitoneal shunt - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Created Date

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