Tissue plasminogen activator-plasminogen activator inhibitor complex (tPA:PAI) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Tissue plasminogen activator-plasminogen activator inhibitor complex (tPA:PAI) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 165648. The device is manufactured by HYPHEN BioMed from France, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Sysmex UK 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
Tissue plasminogen activator-plasminogen activator inhibitor complex (tPA:PAI) IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Oct 17, 2024
Name
Sysmex UK LtdRelationship Type
Address
Sysmex House Garamonde Drive Wymbush
Milton Keynes, Buckinghamshire, England, United Kingdom
Postcode: MK8 8DF
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