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12. ELIA RO60 WELL - INVIMA Registration 5f5c2ca5275ec116a1e8cd42b566ecaf

Access comprehensive regulatory information for 12. ELIA RO60 WELL (12. ELIA RO60 WELL) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 5f5c2ca5275ec116a1e8cd42b566ecaf 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
5f5c2ca5275ec116a1e8cd42b566ecaf
12. ELIA RO60 WELL
INVIMA Analysis ID: 5f5c2ca5275ec116a1e8cd42b566ecaf
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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
5f5c2ca5275ec116a1e8cd42b566ecaf
Expire Date
May 12, 2031
Authorized Company / Fabricante
Name (Spanish)
PHADIA AB
Name (English)
PHADIA AB