2675d0914206d85369dc30227d2764c1

ATELLICA IM HEPATITIS A IGM QUALITY CONTROL (AHAVM QC)

SIEMENS HEALTHCARE S.A.S.·III·Colombia INVIMA·Expires September 14, 2028

Device classification

Risk class / Clase de Riesgo: III
Product type (Spanish): REACTIVO DIAGNOSTICO
Product type (English): DIAGNOSTIC REAGENT

Registration information

Analysis ID: 2675d0914206d85369dc30227d2764c1
Expire date: September 14, 2028

Authorized company / Fabricante

Name (Spanish): SIEMENS HEALTHCARE S.A.S.
Name (English): SIEMENS HEALTHCARE S.A.S.

Product use / Uso del Producto

Spanish

EL ATELLICA IM HEPATITIS A IGM QUALITY CONTROL _x000D_ (AHAVM QC) ESTÁ INDICADO PARA USO DIAGNÓSTICO IN _x000D_ VITRO EN LA MONITORIZACIÓN DE LOS RESULTADOS DEL _x000D_ ENSAYO ATELLICA IM AHAVM CON EL ATELLICA IM _x000D_ ANALYZER

English

THE ATELLICA IM HEPATITIS A IGM QUALITY CONTROL _x000D_ (AHAVM QC) IT IS INDICATED FOR DIAGNOSTIC USE IN _x000D_ VITRO IN MONITORING THE RESULTS OF THE _x000D_ ATELLICA IM AHAVM TEST WITH THE ATELLICA IM _x000D_ ANALYZER

About this record

Access comprehensive regulatory information for ATELLICA IM HEPATITIS A IGM QUALITY CONTROL (AHAVM QC) (ATELLICA IM HEPATITIS A IGM QUALITY CONTROL (AHAVM QC)) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 2675d0914206d85369dc30227d2764c1 and manufactured by SIEMENS HEALTHCARE S.A.S.. The device was registered on September 14, 2028.

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.