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CD59-PE - INVIMA Registration c85f0e90723f856491bd85289a7d7bd5

Access comprehensive regulatory information for CD59-PE (CD59-PE) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID c85f0e90723f856491bd85289a7d7bd5 and manufactured by BECTON DICKINSON DE COLOMBIA LTDA.. The device was registered on April 22, 2034.

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
I
c85f0e90723f856491bd85289a7d7bd5
CD59-PE
INVIMA Analysis ID: c85f0e90723f856491bd85289a7d7bd5
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Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
c85f0e90723f856491bd85289a7d7bd5
Expire Date
April 22, 2034
Authorized Company / Fabricante
Name (English)
BECTON DICKINSON DE COLOMBIA LTDA.