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CD235A-PE - INVIMA Registration 9fcf6d97a12fde17cbbc7c837cdd60cf

Access comprehensive regulatory information for CD235A-PE (CD235A-PE) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 9fcf6d97a12fde17cbbc7c837cdd60cf and manufactured by BECKMAN COULTER COLOMBIA S.A.S.. The device was registered on November 08, 2033.

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
9fcf6d97a12fde17cbbc7c837cdd60cf
CD235A-PE
INVIMA Analysis ID: 9fcf6d97a12fde17cbbc7c837cdd60cf
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
9fcf6d97a12fde17cbbc7c837cdd60cf
Expire Date
November 08, 2033
Authorized Company / Fabricante
Name (English)
BECKMAN COULTER COLOMBIA S.A.S.