Diverting enterostomy re-feeding pump - UK MHRA Medical Device Registration

Diverting enterostomy re-feeding pump is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 87802. The device is manufactured by The Insides Company Limited from New Zealand, classified as General Medical Device. The authorized representative in the UK is Advena 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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Diverting enterostomy re-feeding pump

MHRA Device ID: 87802•Ref: 87802

Device Type

General Medical Device

Devices

Diverting enterostomy re-feeding pump

Type

Class IIb

Date Registered

Apr 11, 2024

Last Updated

Jan 5, 2024

Manufacturer Information

Name

The Insides Company Limited

Address

487 Parnell Road

Auckland, Parnell, New Zealand

Created Date

Jul 7, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

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Other Products from The Insides Company Limited (1)

ENFit/ENFit linear connector

Type: General Medical Device

Registered: Apr 11, 2024

Other Products from Same Authorized Representative (10)

Diverting enterostomy re-feeding pump - UK MHRA Medical Device Registration

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Date Registered

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