T199-402 CA19-9 Rapid Cassette Test (Whole Blood/Serum/Plasma)
- Risk class
- III
- Product type
- In Vitro Diagnostic
- Brand name
- ALLTEST
- Commercial name
- 19-096 IVD Reagents/Kits, Immunoassay, Tumor Marker
- Analysis ID
- f1e0b603397e5202df066621176516be
- Registration date
- November 22, 2023
- Expiration date
- November 22, 2028
- City
- HANGZHOU
- Country
- CHINA
- Address
- #550 TECHNOLOGICAL DEVELOPMENT AREA, HANGZHOU, 310018 ZHEJIANG P. R. CHINA
- Name
- HANGZHOU ALLTEST BIOTECH CO, LTD
- Country
- CHINA
- Address
- AV DE LOS SHYRIS NUMBER: N34-40 AND REPUBLICA DEL SALVADOR
- Phone
- 26009479
A CA19-9 RAPID TEST IN CASSETTE (WHOLE BLOOD/SERUM/PLASMA) IS A RAPID CHROMATOGRAPHIC IMMUNOASSAY FOR THE QUALITATIVE DETECTION OF CA 19-9 IN HUMAN WHOLE BLOOD, SERUM, OR PLASMA. - IN VITRO DIAGNOSTICS
Access comprehensive regulatory information for T199-402 CA19-9 Rapid Cassette Test (Whole Blood/Serum/Plasma) in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID f1e0b603397e5202df066621176516be and manufactured by HANGZHOU ALLTEST BIOTECH CO, LTD. The device was registered on November 22, 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.