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11. ELIA RO52 WELL - INVIMA Registration f90139dd3ef4d8719a4e77a4b038d68e

Access comprehensive regulatory information for 11. ELIA RO52 WELL (11. ELIA RO52 WELL) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID f90139dd3ef4d8719a4e77a4b038d68e 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.

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INVIMA Official Data
II
f90139dd3ef4d8719a4e77a4b038d68e
11. ELIA RO52 WELL
INVIMA Analysis ID: f90139dd3ef4d8719a4e77a4b038d68e
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO

English

DETERMINATION OF ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
f90139dd3ef4d8719a4e77a4b038d68e
Expire Date
May 12, 2031
Authorized Company / Fabricante
Name (Spanish)
PHADIA AB
Name (English)
PHADIA AB