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WL - 31 LEO (II) LYSE - INVIMA Registration 897339321cb6781060198f34c53b25c6

Access comprehensive regulatory information for WL - 31 LEO (II) LYSE (WL - 31 LEO (II) LYSE) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 897339321cb6781060198f34c53b25c6 and manufactured by LABIN COLOMBIA S.A.S. The device was registered on April 24, 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
897339321cb6781060198f34c53b25c6
WL - 31 LEO (II) LYSE
INVIMA Analysis ID: 897339321cb6781060198f34c53b25c6
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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
897339321cb6781060198f34c53b25c6
Expire Date
April 24, 2030
Authorized Company / Fabricante
Name (Spanish)
LABIN COLOMBIA S.A.S
Name (English)
LABIN COLOMBIA S.A.S