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1. M-52 DIFF LYSE - INVIMA Registration 17b7a362ed87e0950ee0ceca61585f5c

Access comprehensive regulatory information for 1. M-52 DIFF LYSE (1. M-52 DIFF LYSE) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 17b7a362ed87e0950ee0ceca61585f5c and manufactured by MINDRAY MEDICAL COLOMBIA SAS. The device was registered on March 01, 2034.

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
17b7a362ed87e0950ee0ceca61585f5c
1. M-52 DIFF LYSE
INVIMA Analysis ID: 17b7a362ed87e0950ee0ceca61585f5c
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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
17b7a362ed87e0950ee0ceca61585f5c
Expire Date
March 01, 2034
Authorized Company / Fabricante
Name (English)
MINDRAY MEDICAL COLOMBIA SAS