CERTUMSYPHILIS/HIV1.2.OCOMBORAPID TEST CASSETTE (WHOLEBLOOD/SERUM/PLASMA) - COFEPRIS Registration 452R2020 SSA
Access comprehensive regulatory information for CERTUMSYPHILIS/HIV1.2.OCOMBORAPID TEST CASSETTE (WHOLEBLOOD/SERUM/PLASMA) (CERTUMSYPHILIS/HIV1.2.OCOMBORAPID TEST CASSETTE (WHOLEBLOOD/SERUM/PLASMA)) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 452R2020 SSA and manufactured by KABLA COMERCIAL, S.A. DEC.V.. The device was registered on April 28, 2020.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
PRUEBA INMUNOCROMATOGRÁFICA RÁPIDAPARALADETECCIÓNDEANTICUERPOSCONTRAVIHTIPO1,TIPO2,SUBTIPOOYANTICUERPOSANTI-SÍFILIS (IGG E IGM) CONTRA TREPONEMAPALLIDUM (TP).
RAPID CHROMATOGRAPHIC IMMUNOASSAY FOR THE DETECTION OF ANTIBODIESCONTRAHIVTYPE1,TYPE2,SUBTYPEOR ANTI-SYPHILIS ANTI-SYPHILIS (IGG AND IGM) ANTI-SYPHILIS (IGG) ANTI-SYPHILIS (IGG) ANTIBODIES.