Spare Parts And Accessories; Electromagnetic Compatibility - Maxtec MaxO2 ME+p Instructions For Use Manual

10.0 SPARE PARTS AND ACCESSORIES
PART NUMBER ITEM
R140P02 Max-550E Sensor
R228P09 Battery Cover
R228P16 Sensor Cable
R228P10 Kickstand
R230M06 MaxO ME+p Operation Manual
2
R207P17 Barbed Concentrator Adapter for Sensor
R205P86 Monitor/Analyzer Wall Mount Bracket
R206P75 Monitor/Analyzer Pole Mount Clamp
RP16P02 Maxtec Approved Tee Adapter (15mm I.D.)
R110P10-001 Sensor Flow Diverter
R230P10 Maxtec Approved External Power Supply
R228P45 Pressure Monitor Port Cover
R229P18-015 Pressure Monitoring Line with Moisture Control Tubing (Qty 15)
Repair of this equipment must be performed by a Maxtec Certified Service Technician experi-
enced in repair of portable hand held medical equipment.
Equipment in need of repair should be sent to:
Maxtec
Service Department
2305 South 1070 West
Salt Lake City, Ut 84119
1.800.748.5355
(Include RMA number issued by Customer Service)
11.0 ELECTROMAGNETIC
COMPATIBILITY
The MaxO2 ME+p is suitable for the electromagnetic environment of typical hospital settings.
The user should assure that it is used in such an environment.
During the immunity testing described below the MaxO2 ME+p will monitor oxygen and pres-
sure within specification.
WARNING: Portable RF communications equipment (including peripherals such as
antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to
any part of the MaxO2 ME+p, including cables specified by the manufacturer. Otherwise,
degradation of the performance of this equipment could result.
WARNING: The MaxO2 ME+p should not be used adjacent to or stacked with other equip-
ment. If adjacent or stacked use is necessary, the MaxO2 ME+p should be observed to
verify normal operation. If operation is not normal, the MaxO2 ME+p or the other equip-
ment should be moved.
WARNING: Use of accessories, transducers and cables other than those specified or
provided by the manufacturer of this equipment could result in increased electromag-
netic emissions or decreased electromagnetic immunity of this equipment and result in
improper operation.
WARNING: Avoid exposure to known sources of EMI (electromagnetic interference) such
as diathermy, lithotripsy, electrocautery, RFID (Radio Frequency Identification), and elec-
tromagnetic security systems such as anti-theft/electronic article surveillance systems,
metal detectors. Note that the presence of RFID devices may not be obvious. If such inter-
ference is suspected, reposition the equipment if possible, to maximize distances.
ENGLISH
ELECTROMAGNETIC EMISSIONS
EMISSION TESTS COMPLIANCE
RF Emissions Group 1
CISPR 11
RF Emissions Class A
CISPR 11
Harmonic Emissions NA
IEC 61000-3-2
Voltage fluctuations NA
/ flicker emissions
IEC 61000-3-3
14
ELECTROMAGNETIC ENVIRONMENT - GUIDANCE
The MaxO2 ME+p uses RF energy only for its
internal function. Therefore, its RF emissions
are very low and are not likely to cause any
interference in nearby electronic equipment.
The MaxO2 ME+p is suitable for use in all
establishments other than domestic, and may
be used in domestic establishments and those
directly connected to the public low-voltage
power supply network that supplies buildings
used for domestic purposes, provided the
following warning is heeded:
WARNING: This equipment/system is intended
for use by healthcare professionals only. This
equipment/ system may cause radio interference
or may disrupt the operation of nearby
equipment. It may be necessary to take mitigation
measures, such as re-orienting or relocating
the MaxO2 ME+p or shielding the location.
WWW.MAXTEC.COM • (800) 748-5355