ZOLL M Series Operator'S Manual Download Page 6

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Warranty (U.S. Only)

(a) ZOLL Medical Corporation warrants to the original 
equipment purchaser that beginning on the date of 
installation, or thirty (30) days after the date of shipment 
from ZOLL Medical Corporation's facility, whichever first 
occurs, the equipment (other than accessories and 
electrodes) will be free from defects in material and 
workmanship under normal use and service for the 
period of one (1) year. During such period ZOLL Medical 
Corporation will, at no charge to the customer, either 
repair or replace (at ZOLL Medical Corporation's sole 
option) any part of the equipment found by ZOLL 
Medical Corporation to be defective in material or 
workmanship. If ZOLL Medical Corporation's inspection 
detects no defects in material or workmanship, ZOLL 
Medical Corporation's regular service charges shall 
apply. (b) ZOLL Medical Corporation shall not be 
responsible for any equipment defect, the failure of the 
equipment to perform any function, or any other 
nonconformance of the equipment, caused by or 
attributable to: (i) any modification of the equipment by 
the customer, unless such modification is made with the 
prior written approval of ZOLL Medical Corporation; (ii) 
the use of the equipment with any associated or 
complementary equipment, (iii) installation or wiring of 
the equipment other than in accordance with ZOLL 
Medical Corporation's instructions, (iv) abuse, misuse, 
neglect or accident. (c) This warranty does not cover 
items subject to normal wear and burnout during use, 
including but not limited to lamps, fuses, batteries, 
patient cables and accessories. (d) The foregoing 
warranty constitutes the exclusive remedy of the 
customer and the exclusive liability of ZOLL Medical 
Corporation for any breach of any warranty related to the 
equipment supplied hereunder. (e) Limitation of Liability: 
ZOLL shall not in any event be liable to Purchaser, nor 
shall Purchaser recover, for special, incidental or 
consequential damages resulting from any breach of 
warranty, failure of essential purpose, or under any other 
legal theory including but not limited to lost profits, lost 
savings, downtime, goodwill, damage to or replacement 
of equipment and property, even if ZOLL has been 
advised of the possibility of such damages. 
THE WARRANTY SET FORTH HEREIN IS EXCLUSIVE 
AND ZOLL MEDICAL CORPORATION EXPRESSLY 
DISCLAIMS ALL OTHER WARRANTIES WHETHER 
WRITTEN, ORAL, IMPLIED, OR STATUTORY, 
INCLUDING BUT NOT LIMITED TO ANY 
WARRANTIES OF MERCHANTABILITY OR FITNESS 
FOR A PARTICULAR PURPOSE. 
For additional information, please call ZOLL Medical 
Corporation at 1-800-348-9011. International customers 
should call the nearest authorized ZOLL Medical 
Corporation service center.

 

Software License

Read this Operator's Manual and License agreement 
carefully before operating any of the M Series products.
Software incorporated into the system is protected by 
copyright laws and international copyright treaties as 
well as other intellectual property laws and treaties. This 
software is licensed, not sold. By taking delivery of and 
using this system, the Purchaser signifies agreement to 
and acceptance of the following terms and conditions:

1.

Grant of License: 

In consideration of payment of the 

software license fee which is part of the price paid for 
this product ZOLL Medical Corporation grants the 
Purchaser a non-exclusive license, without right to 
sublicense, to use the system software in object-code 
form only.

2.

Ownership of Software/Firmware:

 Title to, 

ownership of and all rights and interests in the 
system software and all copies thereof remain at all 
times vested in the manufacturer, and Licensors to 
ZOLL Medical Corporation and they do not pass to 
Purchaser.

3.

Assignment:

 Purchaser agrees not to assign, sub-

license or otherwise transfer or share its rights under 
the license without the express written permission of 
ZOLL Medical Corporation.

4.

Use Restrictions:

 As the Purchaser, you may 

physically transfer the products from one location to 
another provided that the software/firmware is not 
copied. You may not disclose, publish, translate, 
release or distribute copies of the software/firmware 
to others. You may not modify, adapt, translate, 
reverse engineer, decompile, crosscompile, 
disassemble or create derivative works based on the 
software/firmware. 

NO IMPLIED LICENSE

Possession or purchase of this device does not convey 
any express or implied license to use the device with 
replacement parts which would, alone, or in combination 
with this device, fall within the scope of one or more of 
the patents relating to this device. 

Summary of Contents for M Series

Page 1: ...9650 0223 01 Rev D TM End Tidal Carbon Dioxide EtCO2...

Page 2: ...l Corporation CAPNOSTAT is a registered trademark and LoFlo is a trademark of Respironics Novametrix LLC Cidex is a registered trademark of Advanced Sterilization Products a Johnson and Johnson Compan...

Page 3: ...mum filtration of fluids and contaminants and protecting the system from aspiration of these fluids In both systems the CO2 sensor generates infrared light and beams it through the airway adapter or s...

Page 4: ...es EtCO2 option Activate oxygen compensation if O2 levels in excess of 60 are introduced Activate N2O compensation if nitrous oxide is introduced into the airway circuit The presence of Desflurane bey...

Page 5: ...h windows in a vertical NOT a horizontal position This helps keep patient secretions from pooling on the windows Do NOT insert any object other than the sample cell into the sample cell receptacle on...

Page 6: ...t and property even if ZOLL has been advised of the possibility of such damages THE WARRANTY SET FORTH HEREIN IS EXCLUSIVE AND ZOLL MEDICAL CORPORATION EXPRESSLY DISCLAIMS ALL OTHER WARRANTIES WHETHER...

Page 7: ...EtCO2 setup as follows Attaching the CAPNOSTAT 3 sensor cable Selecting a mainstream airway adapter Attaching the airway adapter to the CAPNOSTAT 3 sensor Zeroing the mainstream sensor airway adapter...

Page 8: ...ximately 15 seconds The unit displays the message ZERO DONE upon completion of the zeroing Note Do not attempt zeroing for 20 seconds after removing the adapter from the patient s airway This time all...

Page 9: ...ow steps a through c else go to step 4 a Verify proper connection of the adapter to the sensor b Verify that the airway adapter windows are clean and dry c If the adapter is properly connected and the...

Page 10: ...after its use When the previously used module is reconnected to the M Series unit module zeroing does not have to be repeated as long as no other LoFlo module has been connected and zeroed during the...

Page 11: ...lo module and ensure that it clicks into place 2 If the unit displays either of the following messages take the appropriate action 3 Place the airway adapter assembly at the proximal end of the airway...

Page 12: ...o module and rubber protective covering can be cleaned and disinfected by wiping with one or more of the following solutions 70 isopropyl alcohol 2 gluteraldehyde 10 bleach solution Use a soft cloth d...

Page 13: ...ftkey from the physiological monitoring menu cycles the display from the capnogram waveform to the plethysmograph waveform if SpO2 is installed to no second waveform displayed Use the Zoom softkey fro...

Page 14: ...airway circuit If the concentration of oxygen in the breathing circuit exceeds 60 and nitrous oxide is in use both O2 and N2O should be activated When the Comp softkey is pressed the unit displays the...

Page 15: ...alarm functions are disabled Background ECG analysis functions continue to operate as described in the AED section of the M Series Operator s Guide The ALARM SUSPEND button can be used to activate dea...

Page 16: ...ature unit displays WARM UP message 4 Perform a zero procedure if necessary see Zeroing the LoFlo CO2 Module on page 8 5 Breath normally into the adapter 6 Verify that the unit displays EtCO2 readings...

Page 17: ...3 kPa 0 95 mmHg OFF 0 12 5 OFF 0 12 6 kPa OFF High Respiration Rate Alarm Limit 120 respirations per min 5 150 respirations per min OFF Low Respiration Rate Alarm Limit 5 respirations per min 0 100 re...

Page 18: ...PU Oral Nasal CO2 sampling only pediatric Nasal CO2 Sampling with O2 Delivery Cannula Adult 8000 0356 SPU Nasal CO2 sampling with O2 delivery adult Nasal CO2 Sampling with O2 Delivery Cannula Pediatri...

Page 19: ...problem persists return for service CO2 DEVICE NOT READY The zero operation cannot be initiated because The sensor or module is still warming up No sensor or module is attached to the unit Wait for se...

Page 20: ...g the adapter type Clean airway adapter and reattach it If the problem persists or the adapter type was changed perform a mainstream airway adapter zero as described in Zeroing the Mainstream Sensor A...

Page 21: ...line is set below 0 mmHg Perform a sidestream module zero as described in Zeroing the LoFlo CO2 Module on page 8 CHECK CO2 LINE Sample line blockage Verify that the sample line is plugged into the mod...

Page 22: ...han 5 minutes Replace module ZERO CO2 MODULE Module cable connected to M Series unit for the first time Probe drift error detected or negative CO2 detected Perform module zero as described in Zeroing...

Page 23: ...lt pediatric adapters 50 ms Neonatal adapters 200 ms Respiration Rate Range 0 150 breaths per minute Respiration Rate Accuracy 1 breath per minute Sample Flow Rate N A 50 ml min Compensations Barometr...

Page 24: ...at maximum energy 360J or 1 5 hours minimum of continuous ECG monitoring or 1 0 hour of continuous ECG monitoring pacing at 60 mA 70 beats min For a new fully charged XL battery pack at 20 C 60 defibr...

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