DMEM/NUTRIENT MIXTURE F-12 HAM
- Risk class / Clase de Riesgo
- I
- Product type (Spanish)
- REACTIVOS IN VITRO
- Product type (English)
- REACTIVOS IN VITRO
- Analysis ID
- 76faef02782db1492a3fc94b78765218
- Expire date
- January 10, 2031
- Name (Spanish)
- MERCK S.A.
- Name (English)
- MERCK S.A.
LOS REACTIVOS RUO AMPARADOS EN ESTE REGISTRO _x000D_ SANITARIO SON MEDIOS DE CULTIVO CON SOLUCIONES, _x000D_ SUPLEMENTOS Y SUEROS, CUYA INDICACIÓN DE USO ES _x000D_ SER UTILIZADOS EN CULTIVO CELULAR
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
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.