Pure Global

Epstein-Barr virus (EBV) VCA immunoglobulin G (IgG) antibody avidity index IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Epstein-Barr virus (EBV) VCA immunoglobulin G (IgG) antibody avidity index IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 138289. The device is manufactured by EUROIMMUN Medizinische Labordiagnostika AG from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Euroimmun UK 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 Database
Powered by Pure Global AI
MHRA Registered
In Vitro Diagnostic Device
๐Ÿ‡ฌ๐Ÿ‡ง
Epstein-Barr virus (EBV) VCA immunoglobulin G (IgG) antibody avidity index IVD, kit, enzyme immunoassay (EIA)
MHRA Device ID: 138289โ€ขRef: 138289

Device Type

In Vitro Diagnostic Device

Devices

Epstein-Barr virus (EBV) VCA immunoglobulin G (IgG) antibody avidity index IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 31, 2024

Manufacturer Information

Address

Seekamp 31

Lubeck, Germany

Created Date

May 5, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Ashville House 131-139 The Broadway

Wimbledon, London, England, United Kingdom

Postcode: SW19 1QJ

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing