Equipment Compliance - GE ApexPro Manual

Equipment compliance

IEC, UL, and EN 60601-1 device classification
Type of protection against electrical shock
Degree of protection against electrical
shock
Degree of protection against harmful
ingress of water
Degree of safety of application 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
Mode of operation
1
The T14 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.
2001989-301A- draft 1
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.
2005-08
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
4P41
60601-2-49.
Manufacturer name and address.
European authorized representative.
Transmitter — Internally powered
Receiver system — Class I
T14 transmitter — Type CF Defibrillation proof applied part
T14 transmitter — IPX7 (IEC 60529)
Receiver system — Ordinary Equipment (enclosed equipment without protection against
ingress of water)
Equipment not suitable for use in the presence of a flammable anesthetic mixture with air
or with oxygen or nitrous oxide
Not applicable
Continuous operation
1
ApexPro™
Introduction
1-15