Clostridium difficile antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Clostridium difficile antigen IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 199117. The device is manufactured by TECHLAB, Inc. from United States, classified as In Vitro Diagnostic Device.

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In Vitro Diagnostic Device

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Clostridium difficile antigen IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 199117

Device Type

In Vitro Diagnostic Device

Type

Class B

Status

DREGIY

Date Registered

Aug 20, 2024

Manufacturer Information

Name

TECHLAB, Inc.

Address

2001 Kraft Drive

Blacksburg, Virgina, United States

DJ Fang

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Clostridium difficile antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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