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. - INVIMA Registration 7edfe5ca1cc4312000bd8bc5aaecd6a8

Access comprehensive regulatory information for . (.) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 7edfe5ca1cc4312000bd8bc5aaecd6a8 and manufactured by ABBOTT RAPID DIAGNOSTICS COLOMBIA S.A.S. The device was registered on February 07, 2033.

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
7edfe5ca1cc4312000bd8bc5aaecd6a8
.
INVIMA Analysis ID: 7edfe5ca1cc4312000bd8bc5aaecd6a8
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Product Use / Uso del Producto
Spanish

DETERMINACION 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
7edfe5ca1cc4312000bd8bc5aaecd6a8
Expire Date
February 07, 2033
Authorized Company / Fabricante
Name (English)
ABBOTT RAPID DIAGNOSTICS COLOMBIA S.A.S