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1. CD305-PE - INVIMA Registration dd0d67bf0eeaaafd7e0431edbe6b2143

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.

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INVIMA Official Data
dd0d67bf0eeaaafd7e0431edbe6b2143
1. CD305-PE
INVIMA Analysis ID: dd0d67bf0eeaaafd7e0431edbe6b2143
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Product Use / Uso del Producto
Spanish

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

English

ACTIVE INGREDIENTS FOR IN-HOUSE TECHNIQUES (ASR)

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 (English)
BECKMAN COULTER COLOMBIA SAS