Boditech Quick™ COVID-19 Ag - ARCSA Registration 92161f5f3a67a7d2ba865fe56313ddb4
Access comprehensive regulatory information for Boditech Quick™ COVID-19 Ag in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 92161f5f3a67a7d2ba865fe56313ddb4 and manufactured by BODITECH WITH INC.. The device was registered on May 20, 2023.
This page provides complete registration details including product type (In Vitro Diagnostic), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
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ARCSA Official Data
III
92161f5f3a67a7d2ba865fe56313ddb4
Boditech Quick™ COVID-19 Ag
ARCSA ID: 92161f5f3a67a7d2ba865fe56313ddb4
Device Classification
Risk Class
III
Product Type
In Vitro Diagnostic
Brand Name
Boditech Quick
Commercial Name
64787-SARS-CoV-2 IVD Antigen, Kit, Immunochromatographic Test (ICT), Rapid
Registration Information
Analysis ID
92161f5f3a67a7d2ba865fe56313ddb4
Registration Date
May 20, 2023
Expiration Date
May 20, 2028
Product Use
QUALITATIVE ANTIGEN DETERMINATION OF SARS-COV-2 NUCLEOCAPSID
Manufacturer
City
CHUNCHEON, GANGWON-DO
Country
KOREA, REPUBLIC OF
Address
43, GEODUDANJI 1-GILL, DONGNAE-MYEON, CHUNCHEON-SI, GANGWON DO
Product Owner
Name
BODITECH WITH INC.
Country
KOREA, REPUBLIC OF
Authorized Representative
Address
NEIGHBORHOOD: COOP DE VIVIENDA SERVIDORES Y MANZANA:21 CALLE:AVENIDA JUANTANCA MARENGO, SOLAR 5 INTERSECTION: SN
Phone
42233672