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1. CLINITEK NOVUS PRO 12 URINALYSIS CASSETTE - INVIMA Registration 69eabb257360c2523aa91abe2567e490

Access comprehensive regulatory information for 1. CLINITEK NOVUS PRO 12 URINALYSIS CASSETTE (1. CLINITEK NOVUS PRO 12 URINALYSIS CASSETTE) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 69eabb257360c2523aa91abe2567e490 and manufactured by SIEMENS HEALTHCARE S.A.S. The device was registered on June 11, 2034.

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
69eabb257360c2523aa91abe2567e490
1. CLINITEK NOVUS PRO 12 URINALYSIS CASSETTE
INVIMA Analysis ID: 69eabb257360c2523aa91abe2567e490
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Product Use / Uso del Producto
Spanish

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

English

DETERMINATION OF THE DIFFERENT 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
69eabb257360c2523aa91abe2567e490
Expire Date
June 11, 2034
Authorized Company / Fabricante
Name (English)
SIEMENS HEALTHCARE S.A.S