13c Prueba de aliento con urea para H. Pylori
13c Prueba de aliento con urea para H. Pylori

13c Prueba de aliento con urea para H. Pylori

El principal ingrediente activo del producto es la urea 13C. El frasco contiene 5g/3,3g granulado blanco, muy soluble

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DESCRIPCIÓN

Información básica
N º de Modelo.50 mg/75 mg
Especificaciones.75 mg/50 mg
ClasificaciónDiagnósticos Biológicos
Nº de registroH20061169
Paquete de transporte100 kits en una caja
Especificación75 mg/50 mg
Marca comercialhelicóptero
OrigenPorcelana
Código hs38220090
Descripción del Producto
The main active ingredient of the product is urea 13C. The bottle contains 5g/3.3g white granules, very soluble in water Usage:1. The subjects should fast for at least 4 hours before the examination.2.Fill out the required information on the two sample bags with labeled paper.3.Slowly exhale into the first air bag and make it full of gas as much as possible. Immediately fasten the lid of air bag tightly. This one is the baseline bag (t=0).4.Dissolve the urea 13C granules in 80-100ml cold water, drink it up and sit still for 30 minutes.5. When time up, collect the second breath sample (t=30) like step 3.6. Test the two sample bags with the IR-force infrared spectrometer.Figure:Advantages:1. Non-radioactive, non-toxic to human body, so it is perfect to diagnose children, pregnant women and weak elders.2. First choice for patients who want to evaluate HP radical cure.3. Highly accurate test. Its sensitivity and specificity are relatively high to avoid the possible false-positive and false-negative that may occur in traditional HP diagnoses.4. Non-invasive, so it is easily accepted by patients.5. Diagnoses present HP infection, and reflect full-scaled HP infection status in the stomach.6. Very convenient test: The diagnostic comes out in less than 3 minutes.Clinic applicationAny people who are suspected to have HP infectionPatients who suffer from chronic gastritis, peptic ulcers, gastric cancers or malt lymphomasPatients who have been treated for HP infection and who want to confirm whether the pathogenic bacteria has been eradicated.