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ANTI-S (MONOCLONAL) GAMMA-CLONE, IMMUCLONE - INVIMA Registration 9ecd10e7b2130109dd8a2b930274c1e0

Access comprehensive regulatory information for ANTI-S (MONOCLONAL) GAMMA-CLONE, IMMUCLONE (ANTI-S (MONOCLONAL) GAMMA-CLONE, IMMUCLONE) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 9ecd10e7b2130109dd8a2b930274c1e0 and manufactured by IMMUCOR INC.. The device was registered on April 03, 2030.

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), 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
III
9ecd10e7b2130109dd8a2b930274c1e0
ANTI-S (MONOCLONAL) GAMMA-CLONE, IMMUCLONE
INVIMA Analysis ID: 9ecd10e7b2130109dd8a2b930274c1e0
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Product Use / Uso del Producto
Spanish

DESTINADO A LA DETECCION DEL ANTIGENO S (MNS3), EN GLร“BULOS ROJOS POR PRUEBA DE TUBO.

English

INTENDED FOR THE DETECTION OF ANTIGEN S (MNS3), IN RED BLOOD CELLS BY TUBE TEST.

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
9ecd10e7b2130109dd8a2b930274c1e0
Expire Date
April 03, 2030
Authorized Company / Fabricante
Name (Spanish)
IMMUCOR INC.
Name (English)
IMMUCOR INC.