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N LATEX FLC KAPP - INVIMA Registration 28bf41655c3a64b56b7e261df5c53315

Access comprehensive regulatory information for N LATEX FLC KAPP (N LATEX FLC KAPP) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 28bf41655c3a64b56b7e261df5c53315 and manufactured by SIEMENS HEALTHCARE S.A.S. The device was registered on November 22, 2033.

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
28bf41655c3a64b56b7e261df5c53315
N LATEX FLC KAPP
INVIMA Analysis ID: 28bf41655c3a64b56b7e261df5c53315
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
28bf41655c3a64b56b7e261df5c53315
Expire Date
November 22, 2033
Authorized Company / Fabricante
Name (English)
SIEMENS HEALTHCARE S.A.S