PMC10NCH-GE

GE ApexPro™* CH SpO₂ Nellcor™ Cable

The GE ApexPro™* CH/FH SpO₂ Nellcor™ cables allow for Nellcor™ pulse oximetry to connect to GE ApexPro™* CH/FH transmitters.

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Indications, Safety, and WarningsGE ApexPro™* CH SpO₂-Nellcor™ cableIndications for useThe GE ApexPro™* CH SpO2 – Nellcor cable is indicated for prescription use only for spot-check or continuous non-invasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate. It is intended for use with neonatal, pediatric, and adult patients during both no motion and motion conditions and for patients who are either well or poorly perfused, in hospitals and hospital-type facilities.

Note: Hospital use typically includes such areas as the intensive care unit (ICU), Pediatric Intensive Care Unit (PICU), neonatal intensive care unit (NICU), and medical/surgical general care floor (GCF).

Note: Hospital-type facilities include step-down units and long-term care facilities

Warnings

LOSS OF ALARMS - Do not use transmitter/transceiver accessory devices such as SpO2 and NIBP without ECG cables attached. Failure to use accessory devices in the prescribed manner may result in a loss of alarms

Shock hazard – Do not immerse or wet the SpO2 oximetry cable or sensor

Choking hazard – The SpO2 oximetry cable contains small detachable parts

Cautions

Federal law (U.S.A.) restricts this device to sale by or on the order of a physician.

This device has been tested and found to comply with the limits for medical devices related to IEC 60601-1-2: 2014 for Class B Emissions. These limits are designed to provide reasonable protection against harmful interference in a typical medical installation.

Anyone who connects the SpO2 oximetry cable to a host GE ApexPro™* telemetry system is configuring a medical system and, therefore, is responsible for ensuring the system complies with the Requirements for Medical Electrical Systems IEC/EN 60601-1:2005+A1:2012 and electromagnetic compatibility IEC 60601-1-2:2014

Adverse EventWhile every attempt has been made to reduce patient and operator risk, use of the monitoring cable carries some residual risk. Potential adverse events associated with use of the monitoring cable include, but are not limited to:

Delay of treatment

Choking

Any serious incident that has occurred in relation to the SpO2 oximetry cable should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is establishedSee Instructions for Use for a full list of warnings and cautions GE ApexPro™* FH SpO₂-Nellcor™ cableIndications for useThe GE ApexPro™* FH SpO2 – Nellcor cable is indicated for prescription use only for spot-check or continuous non-invasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate. It is intended for use with neonatal, pediatric, and adult patients during both no motion and motion conditions and for patients who are either well or poorly perfused, in hospitals and hospital-type facilities.

Note: Hospital-type facilities include step-down units and long-term care facilities.

Warnings

Shock hazard – Do not immerse or wet the SpO2 oximetry cable or sensor.

Choking hazard – The SpO2 oximetry cable contains small detachable parts

Cautions

Federal law (U.S.A.) restricts this device to sale by or on the order of a physician.

Anyone who connects the SpO2 oximetry cable to a host GE ApexPro™* FH telemetry system is configuring a medical system and, therefore, is responsible for ensuring the system complies with the Requirements for Medical Electrical Systems IEC/EN 60601-1:2005+A1:2012 and electromagnetic compatibility IEC 60601-1-2:2014.

Delay of treatment

Choking

PMC10NCH-GE

GE ApexPro™* CH SpO₂ Nellcor™ Cable

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United States

Customer Care Team

PMC10NCH-GE GE ApexPro™* CH SpO₂ Nellcor™ Cable

Not what you're looking for?

United States

Customer Care Team

PMC10NCH-GE

GE ApexPro™* CH SpO₂ Nellcor™ Cable