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3. POWERPLEX® 35GY - INVIMA Registration 69d9704c60a4a51a25f444da8fd9426c

Access comprehensive regulatory information for 3. POWERPLEX® 35GY (3. POWERPLEX® 35GY) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 69d9704c60a4a51a25f444da8fd9426c and manufactured by SANITAS S.A.S. The device was registered on August 03, 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
69d9704c60a4a51a25f444da8fd9426c
3. POWERPLEX® 35GY
INVIMA Analysis ID: 69d9704c60a4a51a25f444da8fd9426c
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Product Use / Uso del Producto
Spanish

REACTIVOS PARA EL AISLAMIENTO DE ÁCIDOS NUCLEICOS, SEPARACIÓN Y ANÁLISIS POR FLUORESCENCIA. SOLO PARA USO EN INVESTIGACION

English

REAGENTS FOR NUCLEIC ACID ISOLATION, SEPARATION, AND FLUORESCENCE ANALYSIS. FOR RESEARCH USE ONLY

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
69d9704c60a4a51a25f444da8fd9426c
Expire Date
August 03, 2033
Authorized Company / Fabricante
Name (Spanish)
SANITAS S.A.S
Name (English)
SANITATION S.A.S.