General specimen container IVD, additive/medium - UK MHRA Medical Device Registration

General specimen container IVD, additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 124093. The device is manufactured by FUJIFILM Corporation from Japan, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Fujifilm Healthcare UK Limited.

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General specimen container IVD, additive/medium

MHRA Device ID: 124093•Ref: 124093

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, additive/medium

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Apr 20, 2024

Manufacturer Information

Name

FUJIFILM Corporation

Address

26-30 Nishiazabu 2-chome Minato-ku

Tokyo, Japan

Created Date

Sep 27, 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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Other Products from FUJIFILM Corporation (10)

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General specimen container IVD, additive/medium - UK MHRA Medical Device Registration

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Date Registered

Last Updated

Name

Address

Created Date

Name

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DJ Fang

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