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AQUIOS VERSAFIX LYSING REAGENT - INVIMA Registration 461dda1dea535b77f91d6528af0810d0

Access comprehensive regulatory information for AQUIOS VERSAFIX LYSING REAGENT (AQUIOS VERSAFIX LYSING REAGENT ) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 461dda1dea535b77f91d6528af0810d0 and manufactured by BECKMAN COULTER COLOMBIA S.A.S.. The device was registered on June 05, 2030.

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
I
461dda1dea535b77f91d6528af0810d0
AQUIOS VERSAFIX LYSING REAGENT
INVIMA Analysis ID: 461dda1dea535b77f91d6528af0810d0
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM.

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
461dda1dea535b77f91d6528af0810d0
Expire Date
June 05, 2030
Authorized Company / Fabricante
Name (English)
BECKMAN COULTER COLOMBIA S.A.S.