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Pipette tip IVD - UK MHRA Medical Device Registration

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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MHRA Registered
In Vitro Diagnostic Device
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Pipette tip IVD
MHRA Device ID: 209818

Device Type

In Vitro Diagnostic Device

Type

Class A

Status

DREGIY

Date Registered

Jan 31, 2025

Manufacturer Information

Address

26-30, Nishiazabu 2-chome, Minato-ku

Tokyo, Japan

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