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MODULARDX KIT MSTN EXTRACTION CTR - INVIMA Registration fa685a1a59b823046e680dec4cf6f547

Access comprehensive regulatory information for MODULARDX KIT MSTN EXTRACTION CTR (MODULARDX KIT MSTN EXTRACTION CTR) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID fa685a1a59b823046e680dec4cf6f547 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.

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INVIMA Official Data
I
fa685a1a59b823046e680dec4cf6f547
MODULARDX KIT MSTN EXTRACTION CTR
INVIMA Analysis ID: fa685a1a59b823046e680dec4cf6f547
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Product Use / Uso del Producto
Spanish

LOS REACTIVOS LIGHTMIX RUO AMPARADOS EN ESTE _x000D_ REGISTRO SANITRAIO SON REACTIVOS PARA LA_x000D_ DETECCIร“N Y/O CUANTIFICACIร“N EN MUESTRAS _x000D_ BIOLOGICAS DE ORIGEN HUMANO, DE LOS ACIDOS_x000D_ NUCLร‰ICOS DNA/RNA DE MICROORGANISMOS PATร“GENOS,_x000D_ GENES O MUTACIONES GENETICAS DE LAS Cร‰LULAS

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

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
fa685a1a59b823046e680dec4cf6f547
Expire Date
January 06, 2032
Authorized Company / Fabricante
Name (English)
TIB MOLBIOL SYNTHESELABOR GMBH