1,3-Beta-D-glucan IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

1,3-Beta-D-glucan IVD, kit, nephelometry/turbidimetry is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 164577. 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.

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.

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1,3-Beta-D-glucan IVD, kit, nephelometry/turbidimetry

MHRA Device ID: 164577•Ref: 164577

Device Type

In Vitro Diagnostic Device

Devices

1,3-Beta-D-glucan IVD, kit, nephelometry/turbidimetry

Type

Class C

Date Registered

Nov 26, 2024

Last Updated

Nov 19, 2024

Manufacturer Information

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

DJ Fang

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1,3-Beta-D-glucan IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

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