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DILUENT - INVIMA Registration 8a42fc8c3403274d374c98406701ea09

Access comprehensive regulatory information for DILUENT (DILUENT ) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 8a42fc8c3403274d374c98406701ea09 and manufactured by LABTRONICS S.A.S. The device was registered on April 19, 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
8a42fc8c3403274d374c98406701ea09
DILUENT
INVIMA Analysis ID: 8a42fc8c3403274d374c98406701ea09
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL_x000D_ ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM DEL_x000D_ HUMAN ORGANISM.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
8a42fc8c3403274d374c98406701ea09
Expire Date
April 19, 2032
Authorized Company / Fabricante
Name (Spanish)
LABTRONICS S.A.S
Name (English)
LABTRONICS S.A.S