Pure Global

9. CD13-PC7 - INVIMA Registration ff07f1325eff1679b6653123d48cf1a1

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.

Free Database
Powered by Pure Global AI
INVIMA Official Data
I
ff07f1325eff1679b6653123d48cf1a1
9. CD13-PC7
INVIMA Analysis ID: ff07f1325eff1679b6653123d48cf1a1
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

INGREDIENTES ACTIVOS PARA Tร‰CNICAS IN-HOUSE (ASR)_x000D_

English

ACTIVE INGREDIENTS FOR IN-HOUSE TECHNIQUES (ASR)_x000D_

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 (English)
BECKMAN COULTER COLOMBIA SAS