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3. FLOW CELL (R10.4.1) - INVIMA Registration db486cea2e3f83fafaa49f80adc0d500

Access comprehensive regulatory information for 3. FLOW CELL (R10.4.1) (3. FLOW CELL (R10.4.1)) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID db486cea2e3f83fafaa49f80adc0d500 and manufactured by SUMINISTROS CLINICOS ISLA SAS. The device was registered on June 07, 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
I
db486cea2e3f83fafaa49f80adc0d500
3. FLOW CELL (R10.4.1)
INVIMA Analysis ID: db486cea2e3f83fafaa49f80adc0d500
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Product Use / Uso del Producto
Spanish

PRODUCTOS DISEÑADOS PARA USO EXCLUSIVO EN INVESTIGACIÓN Y NO PARA USO TERAPEUTICO O DIAGNÓSTICO DE_x000D_ SERES HUMANOS O ANIMALES

English

PRODUCTS DESIGNED FOR RESEARCH USE ONLY AND NOT FOR THERAPEUTIC OR DIAGNOSTIC USE DE_x000D_ HUMANS OR ANIMALS

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
db486cea2e3f83fafaa49f80adc0d500
Expire Date
June 07, 2033
Authorized Company / Fabricante
Name (English)
CLINICAL SUPPLIES ISLA SAS