6ea6b3b2b8ac6d81fc0b56eb57e6cfeb

HEMOLYTIC AGENT L

DIAGNOSTILAB VM SAS·II·Colombia INVIMA·Expires August 03, 2033

Device classification

Risk class / Clase de Riesgo: II
Product type (Spanish): REACTIVO DIAGNOSTICO
Product type (English): DIAGNOSTIC REAGENT

Registration information

Analysis ID: 6ea6b3b2b8ac6d81fc0b56eb57e6cfeb
Expire date: August 03, 2033

Authorized company / Fabricante

Name (Spanish): DIAGNOSTILAB VM SAS
Name (English): DIAGNOSTILAB VM SAS

Product use / Uso del Producto

Spanish

DETERMINACIÓN DE LOS DIFERENTES ANALITOS_x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALITOS_x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM.

About this record

Access comprehensive regulatory information for HEMOLYTIC AGENT L (HEMOLYTIC AGENT L) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 6ea6b3b2b8ac6d81fc0b56eb57e6cfeb and manufactured by DIAGNOSTILAB VM SAS. The device was registered on August 03, 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.