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Lumboperitoneal shunt peritoneal catheter - UK MHRA Medical Device Registration

Lumboperitoneal shunt peritoneal catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 78855. The device is manufactured by Medtronic, Inc from United States, classified as General Medical Device. The authorized representative in the UK is Medtronic 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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General Medical Device
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Lumboperitoneal shunt peritoneal catheter
MHRA Device ID: 78855โ€ขRef: 78855

Device Type

General Medical Device

Devices

Lumboperitoneal shunt peritoneal catheter

Type

Class III

Date Registered

Feb 2, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Address

710 Medtronic Parkway

Minneapolis, MN, United States

Created Date

Feb 2, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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