2. E-GEL™ LOW RANGE QUANTITATIVE DNA LADDER - INVIMA Registration 1f5d687d4565a5815ccdbacdc892d5a4
Access comprehensive regulatory information for 2. E-GEL™ LOW RANGE QUANTITATIVE DNA LADDER (2. E-GEL™ LOW RANGE QUANTITATIVE DNA LADDER) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 1f5d687d4565a5815ccdbacdc892d5a4 and manufactured by THERMO FISHER SCIENTIFIC COLOMBIA S.A.S.. The device was registered on June 12, 2034.
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.
EL PRESENTE GRUPO DE REACTIVOS ES UTILIZADO PARA PRODUCTOS COMPLEMENTARIOS PARA BIOLOGÍA MOLECULAR Y SON UTILIZADOS _x000D_ EXCLUSIVAMENTE PARA FINES DE INVESTIGACIÓN (REACTIVOS RUO), NO DEBEN SER UTILIZADOS EN PROCEDIMIENTOS DIAGNÓSTICOS.
THIS GROUP OF REAGENTS IS USED FOR COMPLEMENTARY PRODUCTS FOR MOLECULAR BIOLOGY AND ARE USED _x000D_ EXCLUSIVELY FOR RESEARCH PURPOSES (RUO REAGENTS), THEY SHOULD NOT BE USED IN DIAGNOSTIC PROCEDURES.