United Kingdom MHRA device registration 209817

General specimen container IVD, no additive/medium

United Kingdom·In Vitro Diagnostic Device·FUJIFILM Corporation·Registered Jan 31, 2025DREGIY

Registration details

Device ID: 209817
Status: DREGIY
Date Registered: Jan 31, 2025

Device classification

Device Type: In Vitro Diagnostic Device
Type: Class A

Manufacturer

Name: FUJIFILM Corporation
Address: 26-30, Nishiazabu 2-chome, Minato-ku
Tokyo, Japan

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About this record

General specimen container IVD, no additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 209817. The device is manufactured by FUJIFILM Corporation from Japan, classified as In Vitro Diagnostic Device.

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