376eb6a98e3743db81f61117462d75fe

1. LIGHTMIX MODULAR ENTEROVIRUS 500

TIB MOLBIOL SYNTHESELABOR GMBH·II·Colombia INVIMA·Expires November 24, 2032

Device classification

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

Registration information

Analysis ID: 376eb6a98e3743db81f61117462d75fe
Expire date: November 24, 2032

Authorized company / Fabricante

Name (Spanish): TIB MOLBIOL SYNTHESELABOR GMBH
Name (English): TIB MOLBIOL SYNTHESELABOR GMBH

Product use / Uso del Producto

Spanish

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

English

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

About this record

Access comprehensive regulatory information for 1. LIGHTMIX MODULAR ENTEROVIRUS 500 (1. LIGHTMIX MODULAR ENTEROVIRUS 500) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 376eb6a98e3743db81f61117462d75fe and manufactured by TIB MOLBIOL SYNTHESELABOR GMBH. The device was registered on November 24, 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.