92161f5f3a67a7d2ba865fe56313ddb4
Boditech Quick™ COVID-19 Ag
BODITECH WITH INC.·III·Ecuador ARCSA·Registered May 20, 2023
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
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
Product use
QUALITATIVE ANTIGEN DETERMINATION OF SARS-COV-2 NUCLEOCAPSID
About this record
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.