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RNASE P ASSAY (CY5.5) - INVIMA Registration c5414b97450901d8d4fcb05e83ebd47e

Access comprehensive regulatory information for RNASE P ASSAY (CY5.5) (RNASE P ASSAY (CY5.5) ) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID c5414b97450901d8d4fcb05e83ebd47e and manufactured by AM ASESORIA Y MANTENIMIENTO LTDA. The device was registered on April 25, 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
c5414b97450901d8d4fcb05e83ebd47e
RNASE P ASSAY (CY5.5)
INVIMA Analysis ID: c5414b97450901d8d4fcb05e83ebd47e
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Product Use / Uso del Producto
Spanish

REACTIVOS UE PERMITEN AMPLIFICACION DE MUESTRAS MEDIANTE PCR EN TIEMPO REAL

English

UE REAGENTS ALLOW SAMPLE AMPLIFICATION BY REAL-TIME PCR

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
c5414b97450901d8d4fcb05e83ebd47e
Expire Date
April 25, 2032
Authorized Company / Fabricante
Name (English)
AM ASESORIA Y MANTENIMIENTO LTDA