Pure Global

DIHYDROSTREPTOMYCIN SESQUISULFATE - INVIMA Registration dcb940b23b6da8fe4a272599fd5ec1ca

Access comprehensive regulatory information for DIHYDROSTREPTOMYCIN SESQUISULFATE (DIHYDROSTREPTOMYCIN SESQUISULFATE) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID dcb940b23b6da8fe4a272599fd5ec1ca 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.

Free Database
Powered by Pure Global AI
INVIMA Official Data
I
dcb940b23b6da8fe4a272599fd5ec1ca
DIHYDROSTREPTOMYCIN SESQUISULFATE
INVIMA Analysis ID: dcb940b23b6da8fe4a272599fd5ec1ca
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
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_x000D_

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 ES_x000D_ BE USED IN CELULAR_x000D_ CULTIVATION

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
dcb940b23b6da8fe4a272599fd5ec1ca
Expire Date
January 10, 2031
Authorized Company / Fabricante
Name (Spanish)
MERCK S.A.
Name (English)
MERCK S.A.