United Kingdom MHRA device registration 209818

Pipette tip IVD

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

Registration details

Device ID: 209818
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

Pipette tip IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 209818. The device is manufactured by FUJIFILM Corporation from Japan, classified as In Vitro Diagnostic Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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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