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RaFIA MAU FIA Test - ARCSA Registration d0aa803e5437cea31cad32052129c0c0

Access comprehensive regulatory information for RaFIA MAU FIA Test in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID d0aa803e5437cea31cad32052129c0c0 and manufactured by CTK BIOTECH, INC. The device was registered on March 18, 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.

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ARCSA Official Data
II
d0aa803e5437cea31cad32052129c0c0
RaFIA MAU FIA Test
ARCSA ID: d0aa803e5437cea31cad32052129c0c0
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Device Classification
Risk Class
II
Product Type
In Vitro Diagnostic
Brand Name
CTK Biotech®
Commercial Name
18-902- Reagents/Kits for IVD Assays, Clinical Chemistry, Protein, Albumin, Microalbuminary.
Registration Information
Analysis ID
d0aa803e5437cea31cad32052129c0c0
Registration Date
March 18, 2022
Expiration Date
March 18, 2027
Product Use

FOR IN VITRO DIAGNOSIS: THE MICROALBUMIN FLUORESCENCE IMMUNOASSAY (FIA) TEST IS A FLUORESCENCE CHROMATOGRAPHIC IMMUNOASSAY LATERAL FLOW TEST FOR THE QUANTITATIVE DETECTION OF MAU IN HUMAN URINE,

Manufacturer
City
POWAY
Country
UNITED STATES
Address
13855 STOWE DRIVE
Product Owner
Name
CTK BIOTECH, INC
Country
UNITED STATES
Authorized Representative
Address
URDESA CENTRAL AV. VICTOR EMILIO ESTRADA 917 BETWEEN HIGUERAS AND ILANES
Phone
2881414