Glaucoma shunt - UK MHRA Medical Device Registration

Glaucoma shunt is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 141325. The device is manufactured by Allergan Sales LLC from United States, classified as General Medical Device. The authorized representative in the UK is AbbVie Ltd.

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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Glaucoma shunt

MHRA Device ID: 141325•Ref: 141325

Device Type

General Medical Device

Devices

Glaucoma shunt

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Apr 19, 2024

Manufacturer Information

Name

Allergan Sales LLC

Address

2525 Dupont Drive

Irvine, United States

Created Date

Mar 23, 2022

Authorized Representative

Name

AbbVie Ltd

Relationship Type

UK Responsible Person

Address

AbbVie House Vanwall Business Park Vanwall Road

Maidenhead, Berkshire, United Kingdom

Postcode: SL6 4UB

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Glaucoma shunt - UK MHRA Medical Device Registration

Device Type

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Date Registered

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