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8. PROMETHION FLOW CELL PACKS (R10.4.1) - INVIMA Registration c9878c6ae1f8c52a36487ecd45ab8485

Access comprehensive regulatory information for 8. PROMETHION FLOW CELL PACKS (R10.4.1) (8. PROMETHION FLOW CELL PACKS (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 c9878c6ae1f8c52a36487ecd45ab8485 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
c9878c6ae1f8c52a36487ecd45ab8485
8. PROMETHION FLOW CELL PACKS (R10.4.1)
INVIMA Analysis ID: c9878c6ae1f8c52a36487ecd45ab8485
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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
c9878c6ae1f8c52a36487ecd45ab8485
Expire Date
June 07, 2033
Authorized Company / Fabricante
Name (English)
CLINICAL SUPPLIES ISLA SAS