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Fibrinogen degradation product (FDP) IVD, control - UK MHRA Medical Device Registration

Fibrinogen degradation product (FDP) IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 168452. The device is manufactured by KAMIYA BIOMEDICAL COMPANY, LLC from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Oxford Biosystems Ltd.

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In Vitro Diagnostic Device
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Fibrinogen degradation product (FDP) IVD, control
MHRA Device ID: 168452โ€ขRef: 168452

Device Type

In Vitro Diagnostic Device

Devices

Fibrinogen degradation product (FDP) IVD, control

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Mar 6, 2024

Manufacturer Information

Address

12779 Gateway Drive S.

Tukwila, WA, United States

Created Date

Dec 23, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

184B Park Drive Milton Park Abingdon

Abingdon, Oxfordshire, United Kingdom

Postcode: OX14 4SE

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