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Insulation Tube 300mm with Barb Fittings

733382-HEL-S
733382-HEL
New
Patient Monitoring
Other Patient Monitoring
GE HealthCare
GE HealthCare – Imaging/UL/PCS Parts
GE HealthCare
Total
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Características

  • High quality insulation tube for patient monitoring
  • Excellent ion-conductive
  • Good dimensional stability
  • Highly permeable to water

Descripción del producto

The Insulation Tube 300mm with Barb Fittings is a specially designed tube for patient monitoring. The tube is made up of a high quality Nafion™ material, which is highly ion conductive and functions as a cation exchange polymer. The assembly has a 300 mm preheated Nafion™ tube with stainless steel fitting and injection molded polypropylene barb fitting at both ends of the tube. The sealing surface of the barbs fittings does not contain any parting line and the tube has a good bending radius and can be easily fixed to the patient monitoring system. The insulation tube is calibrated during production to achieve high reliability. The tube material has excellent chemical resistance, which makes it well suited for many medical applications. The products high quality material helps to offer reliable operation, efficient functioning and longer life span.

  • Características adicionales

    • Durable
    • Lightweight
    • Easy to fix
    • Good chemical resistance
    • RoHS compliant

    Artículo equivalente:

    Tenemos las siguientes piezas equivalentes disponibles para usted. Estas son piezas de reemplazo compatibles. Estas piezas sin un hipervínculo se enumeran solo como referencia y no están disponibles para su compra en línea. Para obtener información adicional, comuníquese con el servicio al cliente

    Artículo equivalenteDetalles de parte
    733382-HEL INSUL-TUBE, 300mm +/-10mm, barb fittings, Nafion
    ©2024 GE HealthCare
    JB01359XL
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    Los productos mencionados en este material pueden estar sujetos a regulaciones del gobierno y pueden no estar disponibles en todas las localidades. El embarque y la efectiva comercialización únicamente se podrán realizar si el registro del producto ya ha sido otorgado en su país.