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.
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
Address
1101 Jeter Avenue
Alabama, Opelika, United States
Created Date
Jul 19, 2021
Relationship Type
Address
Caxton Way
Thetford, Norfolk, England, United Kingdom
Postcode: IP24 3SQ
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