GE ApexPro, Operator'S Manual

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Introduction
2001989-200E ApexPro™ 1-17
Equipment compliance
IEC, UL, and EN 60601-1 device classification
This symbol indicates that the waste of electrical and electronic equipment must not be
disposed as unsorted municipal waste and must be collected separately. Please contact an
authorized representative of the manufacturer for information concerning the
decommissioning of your equipment.
This symbol indicates the date of manufacture of this device. The first four digits identify the
year and the last two digits identify the month.
Medical Equipment
With respect to electric shock, fire and mechanical hazards only in accordance with UL
60601-1, CAN/CSA C22.2 NO. 601.1, IEC 60601-1, IEC 60601-1-1, IEC 60601-2-27 and IEC
60601-2-49.
Manufacturer name and address.
European authorized representative.
2005-08
4P41
Type of protection against electrical shock Transmitter — Internally powered
Receiver system — Class I
Degree of protection against electrical
shock ApexPro transmitter — Type CF Defibrillation proof applied part
ApexPro CH transmitter — Type CF Defibrillation proof applied part
Degree of protection against harmful
ingress of water
ApexPro transmitter — IPX3 (IEC 60529)
1
ApexPro CH transmitter — IPX7 (IEC 60529)
2
Receiver system — Ordinary Equipment (enclosed equipment without protection against
ingress of water)
Degree of safety of application in the
presence of a flammable anesthetic
mixture with air or with oxygen or nitrous
oxide Equipment not suitable for use in the presence of a flammable anesthetic mixture with air
or with oxygen or nitrous oxide
Method(s) of sterilization or disinfection
recommended by the manufacturer Not applicable
Mode of operation Continuous operation
1
The ApexPro transmitter is designed to be IPX3 compliant, so it can withstand inadvertent exposure to sprays. The transmitter should not be
exposed to spray or shower during patient monitoring
2
The ApexPro CH transmitter is designed to be IPX7 compliant, so it can withstand inadvertent submersion. The transmitter should not be
exposed to spray or shower during patient monitoring.