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ANALIZADORES RAPIDPOINT DE SIEMENS-ANALIZADOR DE GASES SANGUÍNEOS - INVIMA Registration 1b17c0ab79ca78104ffc3dee376d22c2

Access comprehensive regulatory information for ANALIZADORES RAPIDPOINT DE SIEMENS-ANALIZADOR DE GASES SANGUÍNEOS (SIEMENS RAPIDPOINT ANALYZERS-BLOOD GAS ANALYZER) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 1b17c0ab79ca78104ffc3dee376d22c2 and manufactured by SIEMENS HEALTHCARE SAS. The device was registered on July 19, 2029.

This page provides complete registration details including product type (SURGICAL DOCTOR), 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
IIa
1b17c0ab79ca78104ffc3dee376d22c2
ANALIZADORES RAPIDPOINT DE SIEMENS-ANALIZADOR DE GASES SANGUÍNEOS
INVIMA Analysis ID: 1b17c0ab79ca78104ffc3dee376d22c2
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Product Use / Uso del Producto
Spanish

EL ANALIZADOR DE GASES SANGUÍNEOS RAPIDPOINT 500 PARA SU USO EN LABORATORIOS CLÍNICOS EN DIAGNÓSTICO IN VITRO Y ESTÁ DISEÑADO PARA LA DETERMINACIÓN EN SANGRE TOTAL DE LOS SIGUIENTES PARÁMETROS: PRESIÓN PARCIAL DE DIÓXIDO DE CARBONO; PRESIÓN PARCIAL DE OXÍGENO, PH, SODIO, POTASIO, CALCIO IONIZADO, CLORURO, GLUCOSA, LACTATO, HEMOGLOBINA TOTAL Y FRACCIONES: FOHB, FCOHB, FMETHB, FHHB, BILIRRUBINA NEONATAL._x000D_ LOS SISTEMAS RAPIDPOINT® 500 ESTÁN DISEÑADOS TAMBIÉN PARA LA REALIZACIÓN DE PRUEBAS IN VITRO DE MUESTRAS DE LÍQUIDO PLEURAL CON EL FIN DE OBTENER EL PARÁMETRO PH. EL SISTEMA DE PRUEBA ESTÁ INDICADO PARA SU USO EN ENTORNOS DE LABORATORIO O PUNTOS DE ATENCIÓN AL PACIENTE. LA MEDIDA DEL PH DEL LÍQUIDO PLEURAL PUEDE SER UNA HERRAMIENTA CLÍNICA ÚTIL EN EL TRATAMIENTO DE PACIENTES CON DERRAMES PARANEUMÓNICOS. _x000D_

English

THE RAPIDPOINT 500 BLOOD GAS ANALYZER FOR USE IN CLINICAL LABORATORIES IN IN VITRO DIAGNOSTICS AND IS DESIGNED FOR THE DETERMINATION IN WHOLE BLOOD OF THE FOLLOWING PARAMETERS: PARTIAL PRESSURE OF CARBON DIOXIDE; PARTIAL PRESSURE OF OXYGEN, PH, SODIUM, POTASSIUM, IONIZED CALCIUM, CHLORIDE, GLUCOSE, LACTATE, TOTAL HEMOGLOBIN AND FRACTIONS: FOHB, FCOHB, FMETHB, FHHB, BILIRUBIN NEONATAL._x000D_ THE RAPIDPOINT® 500 SYSTEMS ARE ALSO DESIGNED FOR IN VITRO TESTING OF PLEURAL FLUID SAMPLES TO OBTAIN THE PH PARAMETER. THE TEST SYSTEM IS INDICATED FOR USE IN LABORATORY SETTINGS OR POINTS OF PATIENT CARE. MEASURING PLEURAL FLUID PH MAY BE A USEFUL CLINICAL TOOL IN THE TREATMENT OF PATIENTS WITH PARAPNEUMONIC EFFUSIONS. _x000D_

Device Classification
Risk Class / Clase de Riesgo
IIa
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
1b17c0ab79ca78104ffc3dee376d22c2
Expire Date
July 19, 2029
Authorized Company / Fabricante
Name (English)
SIEMENS HEALTHCARE SAS