Braemar Manufacturing LLC ER920W Manual De Usuario
ER920W Wireless Event Monitor
30
NOTE: This equipment has been tested and found to comply with the
limits for a Class B digital device, pursuant to Part 15 of the FCC Rules.
These limits are designed to provide reasonable protection against
harmful interference in a residential installation. This equipment
generates, uses and can radiate radio frequency energy and, if not
installed and used in accordance with the instructions, may cause harmful
interference to radio communications. However, there is no guarantee
that interference will not occur in a particular installation. If this
equipment does cause harmful interference to radio or television
reception, which can be determined by turning the equipment off and on,
the user is encouraged to try to correct the interference by one or more of
the following measures:
limits for a Class B digital device, pursuant to Part 15 of the FCC Rules.
These limits are designed to provide reasonable protection against
harmful interference in a residential installation. This equipment
generates, uses and can radiate radio frequency energy and, if not
installed and used in accordance with the instructions, may cause harmful
interference to radio communications. However, there is no guarantee
that interference will not occur in a particular installation. If this
equipment does cause harmful interference to radio or television
reception, which can be determined by turning the equipment off and on,
the user is encouraged to try to correct the interference by one or more of
the following measures:
•
Reorient or relocate the receiving antenna.
•
Increase the separation between the equipment and
receiver.
receiver.
•
Connect the equipment into an outlet on a circuit
different from that to which the receiver is connected.
different from that to which the receiver is connected.
•
Consult the dealer or an experienced radio/TV
technician for help.
technician for help.
ER920W Wireless Event Monitor
3
Overview
The ER920W Wireless Event Monitor is a battery operated, solid state,
looping event recorder designed to record symptomatic heart
arrhythmias. Event recording is activated by the patient or by automatic
event detection.
looping event recorder designed to record symptomatic heart
arrhythmias. Event recording is activated by the patient or by automatic
event detection.
The ER920W (1 or 2 channel) event monitor provides up to 30 minutes
of total recording time and will operate as a simple looping event
recorder for a minimum of 30 days with the Lithium Thionyl battery
pack. It offers multiple programmed recording options allowing the
physician to determine their own parameters. Selectable parameters
include number of events, pre-event time, post-event time, audible
operation, pacemaker detection, and arrhythmia detection.
of total recording time and will operate as a simple looping event
recorder for a minimum of 30 days with the Lithium Thionyl battery
pack. It offers multiple programmed recording options allowing the
physician to determine their own parameters. Selectable parameters
include number of events, pre-event time, post-event time, audible
operation, pacemaker detection, and arrhythmia detection.
The ER920W event monitor is enhanced with Arrhythmia Detection
firmware which will capture and automatically record asymptomatic,
infrequent, or elusive heart arrhythmia events such as Bradycardia,
Tachycardia, Pause, and Atrial Fibrillation.
firmware which will capture and automatically record asymptomatic,
infrequent, or elusive heart arrhythmia events such as Bradycardia,
Tachycardia, Pause, and Atrial Fibrillation.
Once an event is recorded, the event ECG is automatically transferred via
a digital cellular link or can be manually transferred transtelephonically
(TTM) via a land line phone.
a digital cellular link or can be manually transferred transtelephonically
(TTM) via a land line phone.
Precautions
A. Patient leads must be removed from electrodes before defibrillation.
B. Observe local laws for disposal of lithium batteries.
C. Do not leave the batteries in the Monitor when it is not in use.
B. Observe local laws for disposal of lithium batteries.
C. Do not leave the batteries in the Monitor when it is not in use.
Damage from corrosion could result.
D. Patient should be instructed to avoid close proximity to heavy
electrical equipment or other sources of electromagnetic
interference.
interference.
E. Use of rechargeable batteries is not recommended.
F. Do not use cellular phone to transmit patient data.
G. Monitor is not for infant use.
H. No automatic analysis algorithm can replace data review by a
F. Do not use cellular phone to transmit patient data.
G. Monitor is not for infant use.
H. No automatic analysis algorithm can replace data review by a
qualified physician. Review and confirmation of analysis results is
required.
required.
Additional equipment classification information as required in EN 60601-1
A. EQUIPMENT not suitable for use in the presence of a
A. EQUIPMENT not suitable for use in the presence of a
FLAMMABLE ANAESTHETIC MIXTURE WITH AIR or WITH
OXYGEN OR NITROUS OXIDE
OXYGEN OR NITROUS OXIDE
B. IPX0 Ordinary Equipment (enclosed equipment without protection
against ingress of water)
C. Internally Powered Equipment
D. Mode of Operation - Continuous Operation
D. Mode of Operation - Continuous Operation