AFIAS FERRITIN - ARCSA Registration c2311f0982b3527800062e4d619f6ae3
Access comprehensive regulatory information for AFIAS FERRITIN in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID c2311f0982b3527800062e4d619f6ae3 and manufactured by BODITECH WITH INC.. The device was registered on September 21, 2018.
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
c2311f0982b3527800062e4d619f6ae3
AFIAS FERRITIN
ARCSA ID: c2311f0982b3527800062e4d619f6ae3
Device Classification
Risk Class
II
Product Type
In Vitro Diagnostic
Brand Name
AFIAS
Commercial Name
IVD Reagents/Assay Kits, Immunoassay, Anemia Assay, Ferritin
Sterilization Method
METHODOLOGY: INMUNOANALISIS
Registration Information
Analysis ID
c2311f0982b3527800062e4d619f6ae3
Registration Date
September 21, 2018
Expiration Date
September 21, 2023
Creation Date
September 21, 2018
Product Use
QUANTIFY FERRITIN IN HUMAN BLOOD / SERUM / PLASMA
Manufacturer
City
CHUNCHEON, GANGWON-DO
Country
KOREA, REPUBLIC OF
Address
43, GEODUDANJI 1-GIL, DONGNAE-MYEON, CHUNCHEON-SI, GANGWON-DO 24398
Product Owner
Name
BODITECH WITH INC.
Country
KOREA, REPUBLIC OF
Authorized Representative
Address
ALBORADA OCTAVA ETAPA CALLE BENJAMIN CARRION SOLAR 5 MANZANA 832 PISO 2 OFICINA 1
Phone
2233672