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RaFIA CRP FIA Test - ARCSA Registration eebbf5eeb87aef1ebb7d34b066554b2c

Access comprehensive regulatory information for RaFIA CRP FIA Test in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID eebbf5eeb87aef1ebb7d34b066554b2c and manufactured by CTK BIOTECH, INC. The device was registered on March 04, 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
eebbf5eeb87aef1ebb7d34b066554b2c
RaFIA CRP FIA Test
ARCSA ID: eebbf5eeb87aef1ebb7d34b066554b2c
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Device Classification
Risk Class
II
Product Type
In Vitro Diagnostic
Brand Name
CTK Biotech®
Commercial Name
17-290 IVD Reagents/Assay Kits, Immunoassay, Protein, C-Reagent
Registration Information
Analysis ID
eebbf5eeb87aef1ebb7d34b066554b2c
Registration Date
March 04, 2022
Expiration Date
March 04, 2027
Product Use

FOR IN VITRO DIAGNOSIS: THE C-REACTIVE PROTEIN FLUORESCENCE IMMUNOASSAY (FIA) TEST IS A FLUORESCENCE CHROMATOGRAPHIC IMMUNOASSAY LATERAL FLOW TEST FOR THE QUANTITATIVE DETECTION OF CRP IN HUMAN SERUM, PLASMA OR BLOOD.

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