5f886f5148cbe433b80e8f28d8b33cff

FERRITIN ELISA DIAMETRA

BIOLORE LTDA·II·Colombia INVIMA·Expires October 06, 2032

Device classification

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

Registration information

Analysis ID: 5f886f5148cbe433b80e8f28d8b33cff
Expire date: October 06, 2032

Authorized company / Fabricante

Name (Spanish): BIOLORE LTDA
Name (English): BIOLORE LTDA

Product use / Uso del Producto

Spanish

FERRITIN ELISA ES UN DISPOSITIVO MANUAL DE DIAGNÓSTICO IN VITRO DESTINADO A LA DETERMINACIÓN CUANTITATIVA DE LA_x000D_ FERRITINA EN SUERO O PLASMA HUMANO. LOS RESULTADOS DEBEN UTILIZARSE COMO AYUDA EN EL DIAGNÓSTICO DE ENFERMEDADES_x000D_ QUE AFECTAN AL METABOLISMO DEL HIERRO JUNTO CON OTROS DATOS CLÍNICOS Y DE LABORATORIO.

English

FERRITIN ELISA IS A HANDHELD IN VITRO DIAGNOSTIC DEVICE INTENDED FOR THE QUANTITATIVE DETERMINATION OF LA_x000D_ FERRITIN IN SERUM OR HUMAN PLASMA. THE RESULTS SHOULD BE USED AS AN AID IN THE DIAGNOSIS OF ENFERMEDADES_x000D_ AFFECTING IRON METABOLISM ALONG WITH OTHER CLINICAL AND LABORATORY DATA.

About this record

Access comprehensive regulatory information for FERRITIN ELISA DIAMETRA (FERRITIN ELISA DIAMETRA) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 5f886f5148cbe433b80e8f28d8b33cff and manufactured by BIOLORE LTDA. The device was registered on October 06, 2032.

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.