Pure Global

BCR-ABCL P210 ELITE MGB KIT - INVIMA Registration da103c99d1bf6c2dba0e31936df43872

Access comprehensive regulatory information for BCR-ABCL P210 ELITE MGB KIT (BCR-ABCL P210 ELITE MGB KIT) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID da103c99d1bf6c2dba0e31936df43872 and manufactured by QUIMIOLAB S.A.S. The device was registered on November 11, 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.

Free Database
Powered by Pure Global AI
INVIMA Official Data
II
da103c99d1bf6c2dba0e31936df43872
BCR-ABCL P210 ELITE MGB KIT
INVIMA Analysis ID: da103c99d1bf6c2dba0e31936df43872
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
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
da103c99d1bf6c2dba0e31936df43872
Expire Date
November 11, 2030
Authorized Company / Fabricante
Name (Spanish)
QUIMIOLAB S.A.S
Name (English)
QUIMIOLAB S.A.S