LIGHTMIX KIT SARS SPIKE N501Y 505H - INVIMA Registration a047d048a6216cd06c0fc84c1b852cc4
Access comprehensive regulatory information for LIGHTMIX KIT SARS SPIKE N501Y 505H (LIGHTMIX KIT SARS SPIKE N501Y 505H) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID a047d048a6216cd06c0fc84c1b852cc4 and manufactured by TIB MOLBIOL SYNTHESELABOR GMBH. The device was registered on July 13, 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 Y MODULARDX RUO AMPARADOS EN ES ESTE REGISTRO SANITARIO SON REACTIVOS PARA LA DETECCIÒN Y/O CUANTIFICACIÓN EN MUESTRAS BIOLOGICAS DE ORIGEN HUMANO, DE LOS ACIDOS NUCLÉICOS DNA/RNA DE MICROORGANISMOS PATÓGENOS, GENES O MUTACIONES GENETICAS DE LA CÉLULAS SOMÁTICAS DE LOS INDIVIDUOS PARA LA DETERMINACIÓN DE UNA CONDICIÓN PARTICULAR. SU PLATAFORMA TECNOLÓGICA ES POR TECNICAS DE BIOLOGIA MOLECULAR POR AMPLIFICACIÓN EN CADENA DE POLIMERASA PCR.
THE LIGHTMIX AND MODULARDX RUO REAGENTS COVERED IN THIS SANITARY REGISTRY ARE REAGENTS FOR THE DETECTION AND / OR QUANTIFICATION IN BIOLOGICAL SAMPLES OF HUMAN ORIGIN, OF THE NUCLEIC ACIDS DNA / RNA OF PATHOGENIC MICROORGANISMS, GENES OR GENETIC MUTATIONS OF THE SOMATIC CELLS OF INDIVIDUALS FOR THE DETERMINATION OF A PARTICULAR CONDITION. ITS TECHNOLOGICAL PLATFORM IS BY MOLECULAR BIOLOGY TECHNIQUES BY PCR POLYMERASE CHAIN AMPLIFICATION.