c2311f0982b3527800062e4d619f6ae3
AFIAS FERRITIN
BODITECH WITH INC.·II·Ecuador ARCSA·Registered September 21, 2018
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
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
Product use
QUANTIFY FERRITIN IN HUMAN BLOOD / SERUM / PLASMA
About this record
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.