Jejunostomy tube - UK MHRA Medical Device Registration

Jejunostomy tube is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99985. The device is manufactured by AbbVie Inc 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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Jejunostomy tube

MHRA Device ID: 99985•Ref: 99985

Device Type

General Medical Device

Devices

Jejunostomy tube

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Aug 29, 2024

Manufacturer Information

Name

AbbVie Inc

Address

1 North Waukegan Road

North Chicago, Illinois, United States

Created Date

Aug 27, 2021

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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Jejunostomy tube - UK MHRA Medical Device Registration

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