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PARVOVIRUS B19 ELITE STANDARD (STD070PLD) - INVIMA Registration 6a79e2b27f2e47f089528b8e2e64d8dd

Access comprehensive regulatory information for PARVOVIRUS B19 ELITE STANDARD (STD070PLD) (PARVOVIRUS B19 ELITE STANDARD (STD070PLD)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 6a79e2b27f2e47f089528b8e2e64d8dd and manufactured by EXOGENA LTDA.. The device was registered on June 23, 2025.

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
6a79e2b27f2e47f089528b8e2e64d8dd
PARVOVIRUS B19 ELITE STANDARD (STD070PLD)
INVIMA Analysis ID: 6a79e2b27f2e47f089528b8e2e64d8dd
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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
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
6a79e2b27f2e47f089528b8e2e64d8dd
Expire Date
June 23, 2025
Authorized Company / Fabricante
Name (Spanish)
EXOGENA LTDA.
Name (English)
EXOGENA LTDA.