United Kingdom MHRA device registration 120585

High density lipoprotein (HDL) cholesterol IVD, reagent

United Kingdom·In Vitro Diagnostic Device·FUJIFILM Wako Pure Chemical Corporation ·Registered Nov 22, 2024

Registration details

Device ID: 120585
MHRA Reference Number: 120585
Date Registered: Nov 22, 2024
Last Updated: Apr 20, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: High density lipoprotein (HDL) cholesterol IVD, reagent
Type: IVD General

Manufacturer

Name: FUJIFILM Wako Pure Chemical Corporation
Address: 1-2 Doshomachi 3-chome
Osaka , Chuoko-ku, Japan
Created Date: Dec 13, 2021

Authorized Representative

Name: Fujifilm Healthcare UK Limited
Relationship Type: UK Responsible Person
Address: Fujifilm House Whitbread Way
Bedford, England, United Kingdom
Postcode: MK42 0ZE

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About this record

High density lipoprotein (HDL) cholesterol IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 120585. The device is manufactured by FUJIFILM Wako Pure Chemical Corporation from Japan, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Fujifilm Healthcare UK Limited.

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