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GAMMA PEG - INVIMA Registration 8c0ed296e95be82ec85799e5c3f6c16b

Access comprehensive regulatory information for GAMMA PEG (GAMMA PEG) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 8c0ed296e95be82ec85799e5c3f6c16b and manufactured by IMMUCOR INC.. The device was registered on January 02, 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
II
8c0ed296e95be82ec85799e5c3f6c16b
GAMMA PEG
INVIMA Analysis ID: 8c0ed296e95be82ec85799e5c3f6c16b
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
8c0ed296e95be82ec85799e5c3f6c16b
Expire Date
January 02, 2030
Authorized Company / Fabricante
Name (Spanish)
IMMUCOR INC.
Name (English)
IMMUCOR INC.