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DMEM/NUTRIENT MIXTURE F-12 HAM - INVIMA Registration 76faef02782db1492a3fc94b78765218

Access comprehensive regulatory information for DMEM/NUTRIENT MIXTURE F-12 HAM (DMEM/NUTRIENT MIXTURE F-12 HAM) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 76faef02782db1492a3fc94b78765218 and manufactured by MERCK S.A.. The device was registered on January 10, 2031.

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
76faef02782db1492a3fc94b78765218
DMEM/NUTRIENT MIXTURE F-12 HAM
INVIMA Analysis ID: 76faef02782db1492a3fc94b78765218
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Product Use / Uso del Producto
Spanish

LOS REACTIVOS RUO AMPARADOS EN ESTE REGISTRO _x000D_ SANITARIO SON MEDIOS DE CULTIVO CON SOLUCIONES, _x000D_ SUPLEMENTOS Y SUEROS, CUYA INDICACIร“N DE USO ES _x000D_ SER UTILIZADOS EN CULTIVO CELULAR

English

THE RUO REAGENTS COVERED BY THIS REGISTER _x000D_ SANITARY ARE CULTURE MEDIA WITH SOLUTIONS, _x000D_ SUPPLEMENTS AND SERUMS, THE INDICATION FOR USE OF WHICH IS _x000D_ BE USED IN CELL CULTURE

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
76faef02782db1492a3fc94b78765218
Expire Date
January 10, 2031
Authorized Company / Fabricante
Name (Spanish)
MERCK S.A.
Name (English)
MERCK S.A.