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DILUENT UNIVERSAL - INVIMA Registration 9c5a8205d2c9a831a64c20b653c29232

Access comprehensive regulatory information for DILUENT UNIVERSAL (DILUENT UNIVERSAL) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 9c5a8205d2c9a831a64c20b653c29232 and manufactured by BIOLORE LTDA. The device was registered on September 20, 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
I
9c5a8205d2c9a831a64c20b653c29232
DILUENT UNIVERSAL
INVIMA Analysis ID: 9c5a8205d2c9a831a64c20b653c29232
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Product Use / Uso del Producto
Spanish

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

English

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

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
9c5a8205d2c9a831a64c20b653c29232
Expire Date
September 20, 2032
Authorized Company / Fabricante
Name (Spanish)
BIOLORE LTDA
Name (English)
BIOLORE LTDA