Borrelia burgdorferi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Borrelia burgdorferi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210135. The device is manufactured by Gold Standard Diagnostics Frankfurt GmbH from Germany, classified as In Vitro Diagnostic Device.

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In Vitro Diagnostic Device

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Borrelia burgdorferi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 210135

Device Type

In Vitro Diagnostic Device

Type

IVD General

Status

DREGIY

Date Registered

Feb 5, 2025

Manufacturer Information

Name

Gold Standard Diagnostics Frankfurt GmbH

Address

Waldstrasse 23 A6

Dietzenbach, Germany

DJ Fang

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Borrelia burgdorferi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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Date Registered

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