Carcinoembryonic antigen (CEA) IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration
Carcinoembryonic antigen (CEA) IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 148704. The device is manufactured by Acro Biotech, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Obelis 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
Carcinoembryonic antigen (CEA) IVD, kit, rapid ICT, clinical
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Apr 13, 2024
Address
4650 Arrow Highway, Suite D-6
Montclair, CA, United States
Created Date
Apr 20, 2021
Name
Obelis UK LtdRelationship Type
Address
Sandford Gate, East Point Business Park
Oxford , England, United Kingdom
Postcode: OX4 6LB
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