dd0d67bf0eeaaafd7e0431edbe6b2143

1. CD305-PE

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

Device classification

Product type (Spanish): REACTIVOS IN VITRO
Product type (English): REACTIVOS IN VITRO

Registration information

Analysis ID: dd0d67bf0eeaaafd7e0431edbe6b2143
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)

English

ACTIVE INGREDIENTS FOR IN-HOUSE TECHNIQUES (ASR)

About this record

Access comprehensive regulatory information for 1. CD305-PE (1. CD305-PE) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID dd0d67bf0eeaaafd7e0431edbe6b2143 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.