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CENTRIFUGA - BECKMAN COULTER - INVIMA Registration e4917667b9c277a64c708b8b51d84299

Access comprehensive regulatory information for CENTRIFUGA - BECKMAN COULTER (CENTRIFUGA - BECKMAN COULTER) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID e4917667b9c277a64c708b8b51d84299 and manufactured by BECKMAN COULTER COLOMBIA S.A.S.. The device was registered on May 17, 2034.

This page provides complete registration details including product type (SURGICAL DOCTOR), 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
e4917667b9c277a64c708b8b51d84299
CENTRIFUGA - BECKMAN COULTER
INVIMA Analysis ID: e4917667b9c277a64c708b8b51d84299
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Product Use / Uso del Producto
Spanish

CENTRIFUGAS MULTIPROPOSITO PARA USO EN LABORATORIO CLINICO. PARA FINES DE SEPARACION DE COMPONENTES POR LA GENERACION DE FUERZA CENTRIFUGA NECESARIA PARA VARIAS APLICACIONES.

English

MULTIPURPOSE CENTRIFUGES FOR USE IN CLINICAL LABORATORY. FOR COMPONENT SEPARATION PURPOSES BY THE GENERATION OF CENTRIFUGAL FORCE NECESSARY FOR VARIOUS APPLICATIONS.

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
e4917667b9c277a64c708b8b51d84299
Expire Date
May 17, 2034
Authorized Company / Fabricante
Name (English)
BECKMAN COULTER COLOMBIA S.A.S.