36bf34d6015b6f9077f8617b48f7a410

10. ELIA MPOS WELL

PHADIA AB·II·Colombia INVIMA·Expires May 12, 2031

Device classification

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

Registration information

Analysis ID: 36bf34d6015b6f9077f8617b48f7a410
Expire date: May 12, 2031

Authorized company / Fabricante

Name (Spanish): PHADIA AB
Name (English): PHADIA AB

Product use / Uso del Producto

Spanish

DETERMINACIÓN DE LOS ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO

English

DETERMINATION OF ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM

About this record

Access comprehensive regulatory information for 10. ELIA MPOS WELL (10. ELIA MPOS WELL) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 36bf34d6015b6f9077f8617b48f7a410 and manufactured by PHADIA AB. The device was registered on May 12, 2031.

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.