- Zoll X Series User Manual
- Zoll M Series Defibrillator Manual
- Zoll M Series User Manual
- Zoll M Series Defibrillator User Manual 2017
- Zoll Defibrillator User Manual
- Zoll M Series Defibrillator For Sale
- M Series Service Manual v Preface Overview ZOLL Medical Corporation’s M Series Service Manual is intended for the ser vice technician who se responsibility is to identify malfunctions and/or make repairs at the subassembly level. The Zoll M Series Service Manual has five main sections and one appendix.
- Find ZOLL product documentation for all ZOLL products. To acquire a copy of the documentation on this site, or if you cannot find the documentation you need, contact our Customer Service Center by calling 01928 241 700 or by sending an e-mail to customerservice-uk@zoll.com. Step 1: Choose product from the list.
Manual Defibrillators; Zoll Defibrillators; Product was successfully added to your shopping cart. Go to cart page Continue Zoll Defibrillators. 4 Item(s) Show: Quick View. Zoll M Series (Recertified) Call for price. Out of stock. Please login to use the compare feature. Zoll E Series (Recertified) Call for price. Out of stock. R Series / Training Accessories. You can flag ZOLL devices you own to simplify compatibility checking. See the User Guide Page for details! Training Accessories. Training Accessories. 7 Item(s) Show Sort By. Set Descending Direction. View and Download ZOLL R Series operator's manual online. The R Series defibrillator also supports ZOLL autoclavable internal handles for use during open chest defibrillation procedures. The R Series does not prevent the user from manually defibrillating the patient. When a shockable rhythm is detected (ventricular. ZOLL R Series Service Manual. If the system shuts down due a slowly depleting battery, the R Series system requires user-intervention to turn back on. This could be due to battery drop- in or the front panel switch. Pediatric Plate Note: The R Series defibrillator also supports ZOLL autoclavable internal handles for use. Find ZOLL ® product documentation for all ZOLL products. To purchase a copy of the documentation on this site, or if you cannot find the documentation you need, contact our Customer Service Center by calling 1-800-348-9011/(978) 421-9655, or by sending an e-mail to info@zoll.com. Step 1: Choose a product from the list.
M S
ERIES
O
PERATOR
’
S
G
UIDE
1-8
Safety Considerations
The M Series products are high energy devices capable
of delivering up to 360 joules. To completely deactivate
the device, you must turn the SELECTOR SWITCH to
the OFF position.
In order to disarm a charged defibrillator:
•
Turn the SELECTOR SWITCH to MONITOR, OFF or
PACER (pacer equipped versions only)
or
•
Change the selected defibrillator energy
As a safety feature, the device will automatically disarm if
left charged for more than 60 seconds (15 seconds for
AED versions).
Note: The terms “ZOLL Multi-Function Electrode (MFE)
Pads” and “MFE Pads” will be used
interchangeably throughout this manual.
WARNINGS
General
•
Federal (U.S.A.) law restricts this device to use by or on
the order of a physician.
•
The use of external pacing/defibrillation electrodes or
adapter devices from sources other than ZOLL is not
recommended. ZOLL makes no representations or
warranties regarding the performance or effectiveness of
its products when used in conjunction with pacing/
defibrillation electrodes or adapter devices from other
sources. Device failures attributable to the use of pacing/
defibrillation electrodes or adapters not manufactured by
ZOLL may void ZOLL's warranty.
•
Proper operation of theunit, together with correct
electrode placement is critical to obtaining optimal
results. Operators must be thoroughly familiar with
proper device operation.
•
Do not use the unit in semiautomatic mode during patient
movement. A patient must be motionless during ECG
analysis. Do not touch the patient during analysis. Cease
all movement via stretcher or vehicle before analyzing
the ECG. If using the device in an emergency vehicle,
bring the vehicle to a halt before using in semiautomatic
mode.
•
Place the patient on a firm surface before performing
CPR.
•
The device is protected against interference from radio
frequency emissions typical of two-way radios and
cellular phones (digital and analog) used in emergency
service/public safety activities. Users should assess the
device’s performance in their typical environment of use
for the possibility of radio frequency interference from
high-power sources. Radio Frequency Interference (RFI)
may be observed as shifts in monitor baseline, trace
compression, display brightness changes or transient
spikes on the display.
•
M Series units equipped with the Bluetooth® option
include an RF transmitter which transmits with 0dBm
power in the 2.4 GHz ISM band.
•
Do not operate the unit without a battery. Keep a fully
charged spare battery pack with the device at all times.
Zoll X Series User Manual
•
Regular use of partially charged battery packs without
fully recharging between uses will result in permanently
reduced capacity and early battery pack failure.
•
Test batteries regularly. Batteries that do not pass ZOLL’s
capacity test could unexpectedly shutdown without
warning.
•
Replace the battery with a fully charged battery
immediately after the “LOW BATTERY” or “REPLACE
BATTERY” message.
•
Emergency defibrillation should be attempted only by
appropriately trained, skilled personnel who are familiar
with equipment operation. Training appropriateness, such
as Advanced Cardiac Life Support (ACLS) or Basic Life
Support (BLS) certification, should be determined by the
prescribing physician.
•
Synchronized cardioversion should only be attempted by
skilled personnel trained in Advanced Cardiac Life
Support (ACLS) and familiar with equipment operation.
The precise cardiac arrhythmia must be determined
before attempting defibrillation.
•
Prior to attempting synchronized cardioversion, ensure
that the ECG signal quality is good and that sync marks
are displayed above each QRS complex.
•
These operating instructions describe the functions and
proper operation of the M Series products. They are not
intended as a substitute for a formal training course.
Operators should obtain formal training from an
appropriate authority prior to using the device for patient
care.
•
Do not disassemble the unit. A shock hazard exists. Refer
all problems to authorized service personnel.
•
Follow all recommended maintenance instructions. If a
problem occurs, obtain service immediately. Do not use
the device until it has been inspected by the appropriate
personnel.
•
Do not use the unit’s ECG out signal as a sync pulse for
another defibrillator or cardioverter.
Zoll M Series Defibrillator Manual
1-1
SECTION 1
GENERAL INFORMATION
Zoll M Series User Manual
NOTE: Your M Series may or may not contain all the features listed in this manual,
depending on your particular configuration.
Product Description
The ZOLL
®
M Series
®
products combine a defibrillator, ECG display, advanced monitoring capabilities, and
Zoll M Series Defibrillator User Manual 2017
Noninvasive Transcutaneous Pacing (NTP) with communication, data printing and recording capabilities in a single
lightweight portable instrument. The unit has been designed for all resuscitation situations and its small, compact,
lightweight design makes it ideal for accompanying patients during transport. The product is powered by AC or DC
mains and an easily replaced battery pack that is quickly recharged in the device when it is connected to AC or DC
mains. In addition, the unit’s batteries may be recharged and tested using ZOLL PowerCharger systems designed for
standard interchangeable ZOLL battery packs.
The product is designed for use in both the hospital and the rugged EMS environment. All of its ruggedized features
add to its durability in hospital applications. The device is a versatile automated external defibrillator with or without
manual capabilities and may be configured to operate in manual, advisory or semi-automated modes. Semi-automated
versions of the device have a distinctive front panel with a single “ON” position. Conventional hospital style devices,
which can be configured for manual, advisory or semi-automated operation, have a standardized ZOLL operator
interface.
When operating in the manual configuration the device operates as a conventional defibrillator where the
device’s charging and discharging is fully controlled by the operator. In advisory and semi-automatic modes, some
features of the device are automated and a sophisticated detection algorithm is used to identify ventricular fibrillation
and determine the appropriateness of defibrillator shock delivery. Units may be configured to automatically charge,
analyze, recharge, and prompt the operator to “PRESS SHOCK,” depending on local protocols. The unit is switched
from the semi-automated mode to manual mode for ACLS use by pressing the appropriate soft key on the front panel.
The M Series assists caregivers during cardiopulminary resuscitation (CPR) by evaluating the rate and depth of chest
compressions, and providing feedback to the rescuer. Real CPR Help™ requires the use of CPR-D•padzand the
CPRD-to-MFC connector. Real CPR Help is available in the M Series unit with software version 38.90 or higher.
Information regarding the unit’s operation, patient ECG, and other physiological waveforms are displayed on a large
5.66 inch diagonal display which provides high contrast and visibility under virtually all lighting conditions. Operating
and warning messages are displayed on the monitor and the unit can also be configured with voice prompts to alert the
user to unit status. Self-diagnostic tests are performed when the instrument is turned on and the unit is periodically
tested during operation.
Zoll Defibrillator User Manual
A sophisticated data collection system, an optional internal summary report feature with printer, and PCMCIA cards are
available for this unit. A PCMCIA card can be installed in the unit to record ECG and virtually all device data when the
device is turned on. In addition, voice data from any incident around this device can also be recorded. The data stored
on the PCMCIA card can be reviewed and archived on a properly equipped personal computer using ZOLL Data
Control™ software.
An annotating stripchart recorder can be included to provide immediate documentation as well as summary report
functions about patient care and treatment during use.
Some M Series products are intended for use in the semiautomatic mode by first responders and emergency medical
technicians certified by an appropriate federal, state or local government authority. Some M Series products are
intended for use in manual mode by personnel certified by appropriate federal, state or local authority to provide
advanced life support care.