ff07f1325eff1679b6653123d48cf1a1

9. CD13-PC7

BECKMAN COULTER COLOMBIA SAS·I·Colombia INVIMA·Expires March 29, 2033

Device classification

Risk class / Clase de Riesgo: I
Product type (Spanish): REACTIVOS IN VITRO
Product type (English): REACTIVOS IN VITRO

Registration information

Analysis ID: ff07f1325eff1679b6653123d48cf1a1
Expire date: March 29, 2033

Authorized company / Fabricante

Name (Spanish): BECKMAN COULTER COLOMBIA SAS
Name (English): BECKMAN COULTER COLOMBIA SAS

Product use / Uso del Producto

Spanish

INGREDIENTES ACTIVOS PARA TÉCNICAS IN-HOUSE (ASR)_x000D_

English

ACTIVE INGREDIENTS FOR IN-HOUSE TECHNIQUES (ASR)_x000D_

About this record

Access comprehensive regulatory information for 9. CD13-PC7 (9. CD13-PC7) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID ff07f1325eff1679b6653123d48cf1a1 and manufactured by BECKMAN COULTER COLOMBIA SAS. The device was registered on March 29, 2033.

This page provides complete registration details including product type (REACTIVOS IN VITRO), 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.