Pure Global

CK-MB - INVIMA Registration 9c45a733d630ecdf00b13df93d029e11

Access comprehensive regulatory information for CK-MB (CK-MB) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 9c45a733d630ecdf00b13df93d029e11 and manufactured by BECKMAN COULTER COLOMBIA S.A.S. The device was registered on June 21, 2027.

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
9c45a733d630ecdf00b13df93d029e11
CK-MB
INVIMA Analysis ID: 9c45a733d630ecdf00b13df93d029e11
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
9c45a733d630ecdf00b13df93d029e11
Expire Date
June 21, 2027
Authorized Company / Fabricante
Name (English)
BECKMAN COULTER COLOMBIA S.A.S