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PT - INVIMA Registration d8d6708408a542717ff5414cf5e428e6

Access comprehensive regulatory information for PT (PT) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID d8d6708408a542717ff5414cf5e428e6 and manufactured by DIAGNOSTILAB VM SAS. The device was registered on December 03, 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
II
d8d6708408a542717ff5414cf5e428e6
PT
INVIMA Analysis ID: d8d6708408a542717ff5414cf5e428e6
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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
d8d6708408a542717ff5414cf5e428e6
Expire Date
December 03, 2030
Authorized Company / Fabricante
Name (Spanish)
DIAGNOSTILAB VM SAS
Name (English)
DIAGNOSTILAB VM SAS