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6. SUPREDYE XT PURIFICATION KIT - INVIMA Registration 001ca1710f59c77ed8b3f02096d2a908

Access comprehensive regulatory information for 6. SUPREDYE XT PURIFICATION KIT (6. SUPREDYE XT PURIFICATION KIT) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 001ca1710f59c77ed8b3f02096d2a908 and manufactured by GENCELL PHARMA SAS. The device was registered on December 29, 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
001ca1710f59c77ed8b3f02096d2a908
6. SUPREDYE XT PURIFICATION KIT
INVIMA Analysis ID: 001ca1710f59c77ed8b3f02096d2a908
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Product Use / Uso del Producto
Spanish

6. EL KIT DE PURIFICACIร“N SUPREDYE XT SECUESTRA LOS_x000D_ COMPONENTES DE LA REACCIร“N DE SECUENCIACIร“N DEL _x000D_ CICLO, COMO IONES DE SAL, TERMINADORES DE TINTE NO_x000D_ INCORPORADOS Y DNTP PARA EVITAR SU COINYECCIร“N _x000D_ CON PRODUCTOS DE EXTENSIร“N MARCADOS CON TINTE _x000D_ EN UN ANALIZADOR DE ADN. LOS REACTIVOS DE_x000D_ PURIFICACIร“N SUPREDYE XT SE PUEDEN PIPETEAR POR _x000D_ SEPARADO Y SECUENCIALMENTE EN LA PLACA DE _x000D_ REACCIร“N, O SE PUEDEN PREMEZCLAR ANTES DE _x000D_ PIPETEAR EN UNA PLACA DE REACCIร“N.

English

6. THE SUPREDYE XT PURIFICATION KIT KIDNAPS LOS_x000D_ COMPONENTS OF THE _x000D_ SEQUENCING REACTION CYCLE, SUCH AS SALT IONS, DYE TERMINATORS NO_x000D_ BUILT-IN AND DNTP TO PREVENT CO-INJECTION _x000D_ WITH EXTENSION PRODUCTS MARKED WITH _x000D_ DYE IN A DNA ANALYZER. THE REAGENTS DE_x000D_ PURIFICATION SUPREDYE XT CAN BE PIPETTE BY _x000D_ SEPARATELY AND SEQUENTIALLY ON THE _x000D_ BOARD REACTION, OR MAY BE PREMIXED BEFORE _x000D_ PIPETTE INTO A REACTION PLATE.

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
001ca1710f59c77ed8b3f02096d2a908
Expire Date
December 29, 2032
Authorized Company / Fabricante
Name (Spanish)
GENCELL PHARMA SAS
Name (English)
GENCELL PHARMA SAS