MODULARDX KIT SCHISTOSOMA - INVIMA Registration fa06226d3540a0b47bb102c35119941c
Access comprehensive regulatory information for MODULARDX KIT SCHISTOSOMA (MODULARDX KIT SCHISTOSOMA) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID fa06226d3540a0b47bb102c35119941c and manufactured by TIB MOLBIOL SYNTHESELABOR GMBH. The device was registered on January 06, 2032.
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.
LOS REACTIVOS LIGHTMIX RUO AMPARADOS EN ESTE _x000D_ REGISTRO SANITRAIO SON REACTIVOS PARA LA_x000D_ DETECCIÓN Y/O CUANTIFICACIÓN EN MUESTRAS _x000D_ BIOLOGICAS DE ORIGEN HUMANO, DE LOS ACIDOS_x000D_ NUCLÉICOS DNA/RNA DE MICROORGANISMOS PATÓGENOS,_x000D_ GENES O MUTACIONES GENETICAS DE LAS CÉLULAS
LIGHTMIX RUO REAGENTS COVERED BY THIS _x000D_ SANITARY REGISTRY ARE REAGENTS FOR LA_x000D_ DETECTION AND/OR QUANTIFICATION IN _x000D_ SAMPLES BIOLOGICAL OF HUMAN ORIGIN, OF THE ACIDOS_x000D_ NUCLEIC DNA/RNA OF PATHOGENIC MICROORGANISMS,_x000D_ GENES OR GENETIC MUTATIONS IN CELLS