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 192139. The device is manufactured by Baxter Healthcare SA from Switzerland, 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: 192139•Ref: 192139

Device Type

General Medical Device

Devices

Hollow-fibre haemodialysis dialyser, single-use

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 16, 2024

Manufacturer Information

Name

Baxter Healthcare SA

Address

Thurgauerstrasse 130 8152 Glattpark Opfikon

Zurich, Switzerland

Created Date

Mar 30, 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

Device Type

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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