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.
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.
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
Address
12779 Gateway Drive S.
Tukwila, WA, United States
Created Date
Dec 23, 2021
Relationship Type
Address
184B Park Drive Milton Park Abingdon
Abingdon, Oxfordshire, United Kingdom
Postcode: OX14 4SE
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