Hollow-fibre haemodialysis dialyser, single-use - UK MHRA Medical Device Registration

Hollow-fibre haemodialysis dialyser, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 89501. The device is manufactured by Gambro Renal Products Inc, trading as Baxter Opelika from United States, classified as General Medical Device. The authorized representative in the UK is Baxter Healthcare 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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Hollow-fibre haemodialysis dialyser, single-use

MHRA Device ID: 89501•Ref: 89501

Device Type

General Medical Device

Devices

Hollow-fibre haemodialysis dialyser, single-use

Type

Class IIb

Date Registered

Jul 19, 2021

Last Updated

Jun 30, 2023

Manufacturer Information

Name

Gambro Renal Products Inc, trading as Baxter Opelika

Address

1101 Jeter Avenue

Alabama, Opelika, United States

Created Date

Jul 19, 2021

Authorized Representative

Name

Baxter Healthcare Ltd

Relationship Type

UK Responsible Person

Address

Caxton Way

Thetford, Norfolk, England, United Kingdom

Postcode: IP24 3SQ

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Hollow-fibre haemodialysis dialyser, single-use - UK MHRA Medical Device Registration

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