f6e4eec19751f7b0fc1127f5c2f9a60a

LIGHTMIX KIT SARS SPIKE S371L S373P

TIB MOLBIOL SYNTHESELABOR GMBH·I·Colombia INVIMA·Expires January 06, 2032

Device classification

Risk class / Clase de Riesgo: I
Product type (Spanish): REACTIVOS IN VITRO
Product type (English): REACTIVOS IN VITRO

Registration information

Analysis ID: f6e4eec19751f7b0fc1127f5c2f9a60a
Expire date: January 06, 2032

Authorized company / Fabricante

Name (Spanish): TIB MOLBIOL SYNTHESELABOR GMBH
Name (English): TIB MOLBIOL SYNTHESELABOR GMBH

Product use / Uso del Producto

Spanish

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

English

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

About this record

Access comprehensive regulatory information for LIGHTMIX KIT SARS SPIKE S371L S373P (LIGHTMIX KIT SARS SPIKE S371L S373P) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID f6e4eec19751f7b0fc1127f5c2f9a60a 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.