Carcinoembryonic antigen (CEA) IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

Carcinoembryonic antigen (CEA) IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 208248. The device is manufactured by SD Biosensor, Inc. from South Korea, classified as In Vitro Diagnostic Device.

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In Vitro Diagnostic Device

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Carcinoembryonic antigen (CEA) IVD, kit, fluorescent immunoassay

MHRA Device ID: 208248

Device Type

In Vitro Diagnostic Device

Type

IVD General

Status

DREGIY

Date Registered

Jan 10, 2025

Manufacturer Information

Name

SD Biosensor, Inc.

Address

C-4th&5th, 16 Deogyeong-daero 1556beon-gil, Yeongtong-gu, Suwon-si, Gyeonggi-do 16690, Republic of Korea

Suwon-si, South Korea

DJ Fang

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Carcinoembryonic antigen (CEA) IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

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Date Registered

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