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ORTHO ANTIBODY ENHANCEMENT SOLUTION - INVIMA Registration c52a35034af310b24c94f544c02112cc

Access comprehensive regulatory information for ORTHO ANTIBODY ENHANCEMENT SOLUTION (ORTHO ANTIBODY ENHANCEMENT SOLUTION ) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID c52a35034af310b24c94f544c02112cc and manufactured by ORTHO - CLINICAL DIAGNOSTICS COLOMBIA S.A.S. The device was registered on December 29, 2032.

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.

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INVIMA Official Data
II
c52a35034af310b24c94f544c02112cc
ORTHO ANTIBODY ENHANCEMENT SOLUTION
INVIMA Analysis ID: c52a35034af310b24c94f544c02112cc
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Product Use / Uso del Producto
Spanish

SOLUCION DE BAJA FUERZA IONICA PARA SU USO EN _x000D_ PRUEBAS DE DETECCION, IDENTIFICACION Y _x000D_ COMPATIBILIDAD DE ANTICUERPOS

English

LOW IONIC STRENGTH SOLUTION FOR USE IN _x000D_ SCREENING, IDENTIFICATION AND _x000D_ TESTING ANTIBODY COMPATIBILITY

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
c52a35034af310b24c94f544c02112cc
Expire Date
December 29, 2032
Authorized Company / Fabricante
Name (English)
ORTHO - CLINICAL DIAGNOSTICS COLOMBIA S.A.S