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HERPES SIMPLEX VIRUS-1 IGG (CLIA) - INVIMA Registration c0d8a3418db201cb131b63757f404ee6

Access comprehensive regulatory information for HERPES SIMPLEX VIRUS-1 IGG (CLIA) (HERPES SIMPLEX VIRUS-1 IGG (CLIA)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID c0d8a3418db201cb131b63757f404ee6 and manufactured by MINDRAY MEDICAL COLOMBIA S.A.S.. The device was registered on December 21, 2033.

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
II
c0d8a3418db201cb131b63757f404ee6
HERPES SIMPLEX VIRUS-1 IGG (CLIA)
INVIMA Analysis ID: c0d8a3418db201cb131b63757f404ee6
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Product Use / Uso del Producto
Spanish

EL ENSAYO DE LA IGG DEL VIRUS DEL HERPES SIMPLE 1 DE LA SERIE CL ES UN INMUNOENSAYO QUIMIOLUMINISCENTE (CLIA) PARA LA DETERMINACIร“N CUALITATIVA DE IGG FRENTE AL VIRUS DEL HERPES SIMPLE TIPO 1 EN SUERO Y PLASMA HUMANOS. LA PRUEBA ESTร DISEร‘ADA PARA COMPLEMENTAR EL DIAGNร“STICO DE UNA INFECCIร“N RECIENTE O ACTUAL CAUSADA POR EL VIRUS DEL HERPES SIMPLE TIPO 1 Y EVALUAR EL ESTADO INMUNITARIO DE PACIENTES, INCLUIDAS LAS MUJERES EMBARAZADAS.

English

THE CL SERIES HERPES SIMPLEX VIRUS 1 IGG ASSAY IS A CHEMILUMINESCENT IMMUNOASSAY (CLIA) FOR THE QUALITATIVE DETERMINATION OF IGG AGAINST HERPES SIMPLEX VIRUS TYPE 1 IN HUMAN SERUM AND PLASMA. THE TEST IS DESIGNED TO SUPPLEMENT THE DIAGNOSIS OF A RECENT OR CURRENT INFECTION CAUSED BY HERPES SIMPLEX VIRUS TYPE 1 AND TO ASSESS THE IMMUNE STATUS OF PATIENTS, INCLUDING PREGNANT WOMEN.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
c0d8a3418db201cb131b63757f404ee6
Expire Date
December 21, 2033
Authorized Company / Fabricante
Name (English)
MINDRAY MEDICAL COLOMBIA S.A.S.