United Kingdom MHRA device registration 189688

Carcinoembryonic antigen (CEA) IVD, kit, chemiluminescent immunoassay

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·Abbott Ireland Diagnostics Division·Registered Nov 26, 2024
Registration details
Device ID
189688
MHRA Reference Number
189688
Date Registered
Nov 26, 2024
Last Updated
May 22, 2024
Device classification
Device Type
In Vitro Diagnostic Device
Devices
Carcinoembryonic antigen (CEA) IVD, kit, chemiluminescent immunoassay
Type
Class C
Manufacturer
Address
Finisklin Business Park
Sligo, Ireland
Created Date
Mar 9, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Abbott House, Vanwall Business Park, Vanwall Road
Maidenhead, Berkshire, England, United Kingdom
Postcode: SL64XE
Similar products

Devices with a matching generic name or device type registered with MHRA

Alpha-fetoprotein (AFP) IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176179
Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176185
Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinicalN/A
Type: In Vitro Diagnostic Device
Manufacturer: Primer Design Ltd
Device ID: 175386
Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176184
C-reactive protein (CRP) IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176164
Cryptosporidium species antigen IVD, kit, rapid ICT, clinicalN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176139
Respiratory syncytial virus (RSV) antigen IVD, kit, rapid ICT, clinicalN/A
Type: In Vitro Diagnostic Device
Manufacturer: Primer Design Ltd
Device ID: 175389
SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testingN/A
Type: In Vitro Diagnostic Device
Manufacturer: Primer Design Ltd
Device ID: 175394
Trichomonas vaginalis antigen IVD, kit, rapid ICT, clinicalN/A
Type: In Vitro Diagnostic Device
Manufacturer: Primer Design Ltd
Device ID: 175395
D-dimer IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176162
Other products from Abbott Ireland Diagnostics Division

Additional devices registered by the same manufacturer

Other products from same authorized representative

Additional devices represented by Abbott Laboratories Limited in the UK

About this record

Carcinoembryonic antigen (CEA) IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 189688. The device is manufactured by Abbott Ireland Diagnostics Division from Ireland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Abbott Laboratories Limited.

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.

Free DatabasePowered by Pure Global AIMHRA RegisteredIn Vitro Diagnostic Device