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Nellcor Nell-3 Printed Wire Assembly (PWA) Pro Series

2030109-001
Patient Monitoring
Patient Monitors
GE Sistemas Médicos de México S.A. de C.V
GE HealthCare
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If you add item(s) to cart and submit your order without the
approval number, GE will contact you before your order
can be confirmed for shipment.

Second Opinion Approval Needed

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Approver Name

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OR

Don't know your approval number? Call 800-437-1171
Enter opt 1 for the first three prompts, and have your System ID available.

If you add item(s) to cart and submit your order without
selecting an approver, GE will contact you before your order
can be confirmed for shipment.


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Características

  • Dimensionally stable
  • Increased life span
  • Low environmental impact
  • Enhanced durability

Descripción del producto

The Nellcor Nell-3 Printed Wire Assembly (PWA) Pro Series is used in the Patient Monitoring. This software provides reliable data during difficult monitoring conditions of low perfusion and interference. This software does not affect the fundamental Indications the use of applicable Nellcor sensors and accessories. The response mode previously allowed the user to specify the averaging technique to optimize measurements in the presence of various patient movements both Mode 1 and Mode 2 is now configured to "Fast Response" as the default setting. The product is securely packaged inside a high quality packing box to avoid physical damage during transit. It is used in a wide range of medical equipment such as Monitoring Subacute Other, Assy DPC400 and other medical diagnostic imaging equipment.

  • Características adicionales

    • Easily portable
    • Lightweight
    • High performance
    • It consumes less amount of power
    • Accurate and sensitive
    • Easy to use
    • Low maintenance required
    • Reliable and durable
    • RoHS compliant
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    2) 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.