STANDARD F Dengue NS1 Ag FIA
- Risk class
- III
- Product type
- In Vitro Diagnostic
- Brand name
- SD BIOSENSOR
- Commercial name
- 17-077 IVD Reagents/Testing Kits, Serology, Viruses
- Analysis ID
- 82c877f7041a7cf00705b0b2862d2559
- Registration date
- December 13, 2022
- Expiration date
- December 13, 2027
- City
- CHUNGCHEONGBUK-DO
- Country
- KOREA, REPUBLIC OF
- Address
- 74, OSONGSAENGMYEONG 4-RO, OSONG-EUP, HEUNGDEOK-GU, CHEONGJU-SI, CHUNGCHEONGBUK-DO 28161, REPUBLIC OF KOREA
- Name
- SD BIOSENSOR, INC.
- Country
- KOREA, REPUBLIC OF
- Name
- SIMED S. A.
- Address
- AV AMAZONAS N37-102 AND NATIONAL UNION OF JOURNALISTS
- Phone
- 2266930
THE STANDARD F DENGUE NS1 AG FIA TEST IS AN IMMUNOFLUORESCENCE ASSAY TO DETECT DENGUE NS1 ANTIGENS IN HUMAN SERUM, PLASMA, OR WHOLE BLOOD SAMPLES.
Access comprehensive regulatory information for STANDARD F Dengue NS1 Ag FIA in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 82c877f7041a7cf00705b0b2862d2559 and manufactured by SD BIOSENSOR, INC.. The device was registered on December 13, 2022.
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.