T-cell intracytoplasmic antigen (TIA1) IVD, antibody - UK MHRA Medical Device Registration
T-cell intracytoplasmic antigen (TIA1) IVD, antibody is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 169984. The device is manufactured by ZETA CORPORATION from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Newmarket Scientific 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
T-cell intracytoplasmic antigen (TIA1) IVD, antibody
Type
IVD General
Date Registered
Mar 25, 2023
Last Updated
Mar 26, 2023
Name
ZETA CORPORATIONAddress
PO Box 282 Sierra Madre
Los Angeles, CA, United States
Created Date
Mar 25, 2023
Relationship Type
Address
9-10 Rosemary House Lanwades Business Park Kennett
Newmarket, Suffolk, England, United Kingdom
Postcode: CB8 7PN
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