CD11A-PE - INVIMA Registration cd4bba7fdc35886c434c5aa73162abf0
Access comprehensive regulatory information for CD11A-PE (CD11A-PE) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID cd4bba7fdc35886c434c5aa73162abf0 and manufactured by BECKMAN COULTER COLOMBIA S.A.S.. The device was registered on January 29, 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
cd4bba7fdc35886c434c5aa73162abf0
CD11A-PE
INVIMA Analysis ID: cd4bba7fdc35886c434c5aa73162abf0
Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
cd4bba7fdc35886c434c5aa73162abf0
Expire Date
January 29, 2034
Authorized Company / Fabricante
Name (Spanish)
BECKMAN COULTER COLOMBIA S.A.S.Name (English)
BECKMAN COULTER COLOMBIA S.A.S.

