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ROTOLAVIT, CELL WASHING CENTRIFUGE - CENTRIFUGA PARA LAVADO CELULAR ROTOLAVIT - INVIMA Registration d663218311a70147635b91cddf42cd3b

Access comprehensive regulatory information for ROTOLAVIT, CELL WASHING CENTRIFUGE - CENTRIFUGA PARA LAVADO CELULAR ROTOLAVIT (ROTOLAVIT, CELL WASHING CENTRIFUGE - CENTRIFUGA PARA LAVADO CELULAR ROTOLAVIT ) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID d663218311a70147635b91cddf42cd3b and manufactured by SYSMEX COLOMBIA S.A.S. The device was registered on June 30, 2031.

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
d663218311a70147635b91cddf42cd3b
ROTOLAVIT, CELL WASHING CENTRIFUGE - CENTRIFUGA PARA LAVADO CELULAR ROTOLAVIT
INVIMA Analysis ID: d663218311a70147635b91cddf42cd3b
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Product Use / Uso del Producto
Spanish

EN EL CASO DEL PRESENTE APARATO SE TRATA DE UNA CENTRรFUGA DE LAVADO QUE ES APROPIADA PARA APLICACIONES DE DIAGNร“STICO IN VITRO, CONFORME A LA DIRECTIVA 98/79 CE. EL PROCESAMIENTO DE LAS PRUEBAS UTILIZANDO EL APARATO Y LOS INSERTOS CORRESPONDIENTES, SE REALIZA LLENANDO CON UN LรQUIDO DE LAVADO Y LUEGO AGITANDO, CENTRIFUGANDO Y DECANTANDO. EL APARATO SIRVE PARA PROCESAMIENTO DE PRUEBAS Y NO PARA ANรLISIS DE PRUEBAS. _x000D_ _x000D_ _x000D_

English

IN THE CASE OF THIS APPARATUS IT IS A WASHING CENTRIFUGE THAT IS SUITABLE FOR IN VITRO DIAGNOSTIC APPLICATIONS, IN ACCORDANCE WITH DIRECTIVE 98/79 EC. THE PROCESSING OF TESTS USING THE APPARATUS AND THE CORRESPONDING INSERTS, IS CARRIED OUT BY FILLING WITH A WASHING LIQUID, AND THEN STIRRING, CENTRIFUGING AND DECANTING. THE APPARATUS IS USED FOR TEST PROCESSING AND NOT FOR TEST ANALYSIS. _x000D_ _x000D_ _x000D_

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
d663218311a70147635b91cddf42cd3b
Expire Date
June 30, 2031
Authorized Company / Fabricante
Name (Spanish)
SYSMEX COLOMBIA S.A.S
Name (English)
SYSMEX COLOMBIA S.A.S