db486cea2e3f83fafaa49f80adc0d500

3. FLOW CELL (R10.4.1)

SUMINISTROS CLINICOS ISLA SAS·I·Colombia INVIMA·Expires June 07, 2033

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 (Spanish): SUMINISTROS CLINICOS ISLA SAS
Name (English): CLINICAL SUPPLIES ISLA SAS

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

About this record

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.