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AMPLIRUN® EPSTEIN-BARR VIRUS DNA CONTROL - INVIMA Registration 6ec29ed41f29fd461c634563fb5c2402

Access comprehensive regulatory information for AMPLIRUN® EPSTEIN-BARR VIRUS DNA CONTROL (AMPLIRUN® EPSTEIN-BARR VIRUS DNA CONTROL) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 6ec29ed41f29fd461c634563fb5c2402 and manufactured by ANNAR DIAGNOSTICA IMPORT S.A.S..

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), 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
III
6ec29ed41f29fd461c634563fb5c2402
AMPLIRUN® EPSTEIN-BARR VIRUS DNA CONTROL
INVIMA Analysis ID: 6ec29ed41f29fd461c634563fb5c2402
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Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
6ec29ed41f29fd461c634563fb5c2402
Authorized Company / Fabricante
Name (English)
ANNAR DIAGNOSTICA IMPORT S.A.S.