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DAC-510E-EN-BF

ORIGINAL END USER’S LIMITED WARRANTY*

COVERAGE

Defibtech, LLC provides a limited warranty that the defibrillator 

and its associated accessories (e.g., batteries and pads), 

whether purchased concurrently with the defibrillator as part 

of a configuration or separately, shall be substantially free 

from defects in material and workmanship.  Defibtech’s limited 

warranty shall only extend to the original end user, where 

the original end user purchased the items from an authorized 

Defibtech, LLC retailer.  This limited warranty may not be 

assigned or transferred.  The terms of the Limited Warranty 

in effect as of the date of original purchase shall apply to any 

warranty claims.

LENGTH  OF WARRANTY

The defibrillator’s limited warranty is for a period of eight (8) 

years from the date of purchase.  The battery’s limited warranty 

is for a period of four (4) years from the date of purchase, but in 

no event shall the limited warranty period extend past the date 

printed on the battery.  Single use accessories (e.g., the pads) 

shall have a limited warranty up to use or for a period up to the 

expiration date, whichever is earlier.  The limited warranty for 

all other accessories is for a period of one (1) year from the 

date of purchase, or to the expiration date, whichever is earlier.

LIMITED WARRANTY  LIMITATIONS

This limited warranty does not cover damage of any sort 

resulting from, but not limited to, accidents, improper 

storage, improper operation, alterations, unauthorized service, 

tampering, abuse, neglect, fire, flood, war, or acts of God.  

Additionally, this limited warranty does not cover damage 

of any sort to the defibrillator or its associated accessories 

resulting from the use of the defibrillator with unapproved 

accessories or use of the accessories with unapproved medical 

devices.  The defibrillator and its associated accessories are 

not warranted to be compatible with any other medical device.

LIMITED WARRANTY VOIDED

The limited warranty is immediately voided if:  the defibrillator 

or its associated accessories are serviced or repaired by any 

entity,  including  persons,  not  authorized  by  Defibtech,  LLC; 

specified maintenance is not performed; the defibrillator 

is  used  with  one,  or  more,  unauthorized  accessories;  the 

associated  accessories  are  used  with  an  unauthorized 

defibrillator; or the defibrillator or associated accessories 

are not used in accordance with Defibtech, LLC approved 

instructions.

EXCLUSIVE REMEDY

At Defibtech, LLC’s sole discretion, Defibtech shall have the 

option to repair, replace, or provide a credit.  In the event 

of replacement, Defibtech shall have the right at its sole 

discretion to replace the item with a new, or refurbished, same 

or similar item.  Determination of a similar item shall be at 

the sole discretion of Defibtech.  In the case of replacement, 

the replacement at a minimum shall reflect the prorated 

time remaining for the item based on the remaining limited 

warranty period.  In the case of a credit, the credit shall be the 

prorated value of the item based on the lower of the original 

item cost of the same or similar item and the remaining limited 

warranty period.  In no event, shall the limited warranty period 

of a replacement item extend past the limited warranty period 

of the item it is replacing.

WARRANTY SERVICE

In order to obtain warranty service, contact the retailer from 

whom the item was purchased, or Defibtech, LLC customer 

service.    In  the  event  an  item  must  be  returned,  a  Return 

Material  Authorization  (RMA)  number  is  required.    Items 

returned without an RMA number will not be accepted.  The 

item shall be shipped at the original end user’s expense to a 

destination specified by the retailer or Defibtech, LLC.

OBLIGATIONS AND WARRANTY  LIMITS

THE  FOREGOING  LIMITED  WARRANTY  IS  IN  LIEU  OF 

AND  SPECIFICALLY  EXCLUDES  AND  REPLACES,  TO  THE 

DEGREE  PERMITTED  BY  APPLICABLE  STATE  LAW,  ALL 

OTHER  EXPRESS  OR  IMPLIED WARRANTIES,  INCLUDING, 

BUT  NOT  LIMITED  TO,  THE  IMPLIED  WARRANTIES  OF 

MERCHANTABILITY  AND  FITNESS  FOR  A  PARTICULAR 

PURPOSE.

NO  PERSON  (INCLUDING  ANY  AGENT,  DEALER,  OR 

REPRESENTATIVE  OF  DEFIBTECH,  LLC)  IS  AUTHORIZED 

TO  MAKE  ANY  REPRESENTATION  OR  WARRANTY 

CONCERNING  THE  DEFIBRILLATOR  OR  ITS  ASSOCIATED 

ACCESSORIES,  EXCEPT  TO  REFER  TO  THIS  LIMITED 

WARRANTY.

THE  EXCLUSIVE  REMEDY  WITH  RESPECT  TO  ANY  AND 

ALL  LOSSES  OR  DAMAGES  RESULTING  FROM  ANY 

CAUSE  WHATSOEVER  SHALL  BE  AS  SPECIFIED  ABOVE.  

DEFIBTECH, LLC SHALL IN NO EVENT BE LIABLE FOR ANY 

CONSEQUENTIAL OR INCIDENTAL DAMAGES OF ANY KIND, 

INCLUDING, BUT NOT LIMITED TO, EXEMPLARY DAMAGES, 

SPECIAL,  PUNITIVE,  COMMERCIAL  LOSS  FROM  ANY 

CAUSE, BUSINESS INTERRUPTION OF ANY NATURE, LOSS 

OF  PROFITS  OR  PERSONAL  INJURY,  EVEN  IF  DEFIBTECH, 

LLC HAS BEEN ADVISED OF THE POSSIBILITIES OF SUCH 

DAMAGES,  HOWEVER  OCCASIONED,  WHETHER  BY 

NEGLIGENCE OR OTHERWISE, UNLESS APPLICABLE STATE 

LAW DOES NOT ALLOW SUCH EXCLUSION OR LIMITATION.

11  Warranty Information

*Applicable to defibrillators and associated accessories 

having a date of manufacture on or after January 1, 2013. 

For all others, refer to warranty information in effect at the 

time of manufacture.

Содержание Lifeline/ReviveR DDU-100

Страница 1: ...Defibtech DDU 100 Semi Automatic External Defibrillator User Manual AHA ERC 2010 DAC 510E EN BF ELECTRONIC DISTRIBUTION...

Страница 2: ......

Страница 3: ...iii DAC 510E EN BF...

Страница 4: ...s are fictitious unless otherwise noted Limited Warranty The Limited Warranty shipped with Defibtech AED products serves as the sole and exclusive warranty provided by Defibtech LLC with respect to th...

Страница 5: ...Maintenance 7 2 2 Improper Device Performance 7 2 2 1 Usage Environment 7 2 2 2 Pads 8 2 2 3 Patient Analysis 8 2 2 4 Shock Delivery 9 2 2 5 Maintenance 9 2 3 General 10 3 Setting up the DDU 100 AED 1...

Страница 6: ...ive Status Indicator 30 5 2 2 Checking the Condition of the Unit and Accessories 31 5 2 3 Running a Manually Initiated Self Test 32 5 2 4 Replacing Pads 32 5 2 5 Checking Pad and Battery Pack Expirati...

Страница 7: ...teria 50 8 1 5 2 Patient Analysis System Performance 51 8 1 6 Clinical Summary 51 8 1 6 1 Background 51 8 1 6 2 Methods 52 8 1 6 3 Results 52 8 1 6 4 Conclusion 52 8 1 7 Guidance and Manufacturer s De...

Страница 8: ...viii DAC 510E EN BF...

Страница 9: ...present Charges the defibrillation capacitor and arms the SHOCK button if the AED detects a shockable rhythm Prompts the operator to press the SHOCK button when the device is ready and a shock is rec...

Страница 10: ...ally on Defibtech Data Cards DDC The optional DDC plugs into a slot in the AED and enables the AED to record event documentation and audio audio enabled cards only if sufficient space is available on...

Страница 11: ...ASI When the unit is off this indicator blinks green to indicate the unit is fully operational and blinks red to indicate unit needs attention from the user or servicing L Patient pads The defibrilla...

Страница 12: ...indications The DDU 100 AED should not be used if the patient shows any of the following signs Conscious and or responsive Breathing Has a detectable pulse 1 5 OperatorTraining Requirements In order t...

Страница 13: ...t in serious personal injury or death CAUTION Conditions hazards or unsafe practices that may result in minor personal injury damage to the DDU 100 AED or loss of data 2 1 Shock Fire Hazard Explosion...

Страница 14: ...le substance air mixtures CAUTION Do not immerse any portion of this product in water or other fluids Do not allow fluids to enter the device Avoid spilling any fluids on this device or accessories Sp...

Страница 15: ...and metal objects which may provide unwanted pathways for defibrillating current 2 1 5 Maintenance WARNING Electrical shock hazard Dangerous high voltages and currents are present Do not open unit re...

Страница 16: ...ient Analysis WARNING Aggressive or prolonged CPR to a patient with defibrillation pads attached can cause damage to the pads Replace the defibrillation pads if they become damaged during use WARNING...

Страница 17: ...patient skin burns To help prevent air pockets make sure self adhesive defibrillation pads completely adhere to the skin Do not use dried out or expired defibrillation pads 2 2 5 Maintenance WARNING...

Страница 18: ...10 DAC 510E EN BF 2 3 General CAUTION Federal law USA restricts this device to sale by or on the order of a physician...

Страница 19: ...are required to begin using the device 3 1 Overview The following components and accessories are included with your DDU 100 AED Replacement and other accessories are detailed in the DDU 100 AED Acces...

Страница 20: ...Active Status Indicator 9V Battery A user replaceable lithium 9V battery located inside the battery pack provides Active Status Indicator ASI power This auxiliary battery is used to provide standby in...

Страница 21: ...nstall the battery pack after the expiration date printed on the label The battery pack is non rechargeable A green Active Status Indicator on the label side of the battery pack will blink periodicall...

Страница 22: ...ng should be opened only immediately prior to use otherwise the pads may dry out and become non functional Note The DDU 100 AED is designed to be stored with the pads connector already installed This...

Страница 23: ...om The user should refer to the Troubleshooting section in Chapter 5 of this manual for appropriate action Note Every time the manually initiated Self Test is run the unit does an internal shock test...

Страница 24: ...16 DAC 510E EN BF...

Страница 25: ...and prompts guide the operator through the use of the unit The following sections describe in detail how to use the DDU 100 AED The basic steps for use are Turn the DDU 100 AED ON by pressing the ON...

Страница 26: ...mally Active Status Indicator Off Battery pack not installed AED is defective or the 9V battery is discharged Install functional battery pack or replace the 9V battery in the battery pack Steady On gr...

Страница 27: ...ackage Pull the protective backing from the pads and check that the pads are Free from obvious signs of damage Clean of excessive debris for example dirt if the pad was dropped Not dried out and that...

Страница 28: ...he dotted line near the top of the package Remove the pads from the package and follow the directions and diagram showing proper defibrillation pad placement located on the defibrillation pad package...

Страница 29: ...patient s bare chest as shown This indicates that the DDU 100 AED has determined that the pads are not placed on the patient Place pads on the patient following instructions on the pad package If the...

Страница 30: ...erference related voice prompts Stop motion This indicates that the DDU 100 AED has detected motion in the patient Stop all patient motion including CPR in response to this message If the patient is b...

Страница 31: ...ised This indicates that the DDU 100 AED has determined that a shock is not required The unit will not charge and the SHOCK button will not be enabled The user will be prompted to begin CPR if needed...

Страница 32: ...r a shock The operator should press the SHOCK button to deliver the shock The Shock button will flash during this phase SHOCK Off No Shock indicated Button is disabled pressing the button will do noth...

Страница 33: ...te to perform CPR If needed begin CPR This indicates that the user should begin CPR if needed for two minutes The unit will not be monitoring the patient s ECG rhythm during this two minute CPR period...

Страница 34: ...conds or Continue for 1 minute x seconds This indicates that the user should continue performing CPR for x more seconds or for 1 minute and x more seconds respectively The unit will not be monitoring...

Страница 35: ...asses Connect a new pad package check to make sure the package is not expired Hold ON OFF button down for at least five seconds to initiate a manually initiated Self Test Unit will report status of th...

Страница 36: ...28 DAC 510E EN BF...

Страница 37: ...nd no voltage will be present at the pads at any time Note Every time the manually initiated Self Test is run the unit does an internal shock test This test reduces the capacity of the battery pack by...

Страница 38: ...t is flashing red or not flashing at all the AED needs attention Anytime the ASI is flashing red and a good 9V battery is installed the unit will periodically emit a beep to call attention to itself I...

Страница 39: ...ken Replace battery pack This indicates that the battery pack is almost discharged and that the AED may not be able to deliver defibrillation shocks The battery pack should be replaced immediately Rep...

Страница 40: ...the ON OFF button again If the Self Test fails The user should refer to the Troubleshooting section in Chapter 5 of this manual 5 2 4 Replacing Pads The Defibtech defibrillation monitoring pads are in...

Страница 41: ...an accessory is past its expiration date it should be replaced immediately Follow the instructions in the Installing and Removing the Battery Pack and Connecting the Pads sections to replace the part...

Страница 42: ...of the 9V battery compartment Replace the 9V battery compartment door by reversing the process used to remove the door If the battery pack is stored out of the AED for an extended period of time remo...

Страница 43: ...cket Soapy water Ammonia based cleaners Hydrogen peroxide Isopropyl alcohol 70 percent solution Chlorine bleach 30 ml liter water Ensure that the connector socket is completely dry before reinstalling...

Страница 44: ...ibtech DDU 100 Operator s Checklist Defibtech DDU 100 Serial Number ___________________________________________________ Defibtech DDU 100 Location _____________________________________________________...

Страница 45: ...rode pads are not pre connected to unit Connect electrode pads to unit ASI does not blink at all ASI 9V battery depleted Replace ASI 9V battery Battery pack not inserted Insert battery pack Battery pa...

Страница 46: ...as been detected Stop external interference Analyzing interrupted voice prompt Motion or interference detected Stop motion or interference Shock cancelled voice prompt Patient s ECG rhythm changed No...

Страница 47: ...39 DAC 510E EN BF 5 8 Repair The DDU 100 AED contains no user serviceable parts If the unit need servicing return to an authorized service center Refer to Contacts section for contact information...

Страница 48: ...40 DAC 510E EN BF...

Страница 49: ...stored with pads connected When the DDU 100 AED is used the operator needs only to remove the pad packaging tear open the package and turn the device on to administer care The AED has a storage area i...

Страница 50: ...to prevent the main defibrillation battery from being depleted for non essential functions This provides a significantly longer standby life for the AED and battery pack and extends the lifetime durin...

Страница 51: ...us event will NOT be erased If the DDC fills completely the AED will still be operable and the most critical event documentation for the current session is still recorded internally Internally recorde...

Страница 52: ...tronic Equipment EEE may contain polluting components and hazardous substances the accumulation of which could pose serious risk for the environment and human health It is for this reason that local A...

Страница 53: ...tioning DefibView is a stand alone software application It cannot be used with the AED in operation and exists solely to support post event review of the data recorded on a DDC or downloaded to a DDC...

Страница 54: ...ately after each shock and all ECG data during the charging and waiting to shock periods Note Audio data is not logged internally To download the internally logged information perform the following pr...

Страница 55: ...0F 516 5 Procedure IV 1 meter any edge corner or surface in standby mode Vibration MIL STD 810F 514 5 Category 20 RTCA DO 160D Section 8 8 2 Cat R Zone 2 Curve G Helicopter RTCA DO 160D Section 8 Cat...

Страница 56: ...utton voice prompt Shock delivery Shock is delivered by a single SHOCK button DISARM Automatic If Patient Analysis System decides rhythm is no longer shockable or Within 30 seconds after Charge comple...

Страница 57: ...es that the pad patient impedance is within the proper range and analyzes the patient s ECG rhythm to determine whether a shock is required On detection of a non shockable rhythm the user is prompted...

Страница 58: ...low amplitude or low frequency VF rhythms may not be interpreted as shockable VentricularTachycardia including ventricular flutter and polymorphic VT Cardiac rhythm rate of at least 180 bpm and peak...

Страница 59: ...rnal Defibrillators for Public Access Defibrillation Recommendations for Specifying and Reporting Arrhythmia Analysis Algorithm Performance Incorporating New Waveforms and Enhancing Safety American He...

Страница 60: ...nd biphasic groups in terms of age sex weight primary structural heart diseases cause or location of arrest bystanders who witnessed the arrest or type of responder A summary of the results is present...

Страница 61: ...ble for use in all establishments including domestic establishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Harmo...

Страница 62: ...ymbol Note 1 At 80 MHz and 800 MHz the higher frequency range applies Note 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from...

Страница 63: ...For transmitters rated at a maximum output power not listed above the recommended separation distance d in meters m can be determined using the equation applicable to the frequency of the transmitter...

Страница 64: ...de Disposable recyclable non rechargeable ASI battery standby life after installation 1 year typical new battery at 25 C 8 2 2 Standard Lithium Battery Pack Category Specification Model number DBP 140...

Страница 65: ...urns 8 4 Defibtech Data Cards DDCs Use only Defibtech Data Cards in the DDU 100 AED Defibtech Data Cards are available as follows Standard DDCs Model Number Details DDC 6 Up to 6 hours of ECG data DDC...

Страница 66: ...on various Windows platforms including Windows 98 Windows 2000 and Windows XP Minimum system requirements for adequate performance are as follows Pentium II Processor at 300 MHz 32 Mbyte System Memory...

Страница 67: ...the device when it is charged and then turns the device OFF X X X X Y Y Y Y Do not expose to high heat or open flame Do not incinerate X X X X Y Y Y Y Recyclable X X X X Y Y Y Y Consult operating ins...

Страница 68: ...of BF type patient applied parts per EN 60601 1 Y Y Y Y Manufacturer Y Y Y Y Date of manufacture Y Y Y Y Do not reuse Y Y Y Y For USA users only Y Y Y Y Catalogue number Keep dry Handle with care Tran...

Страница 69: ...ctric shock fire and mechanical hazard only in accordance with UL 60601 1 CAN CSA C22 2 No 601 1 M90 IEC 60601 1 and IEC 60601 2 4 Conforms to UL Standard UL 60601 1 Certified to CAN CSA Standard C22...

Страница 70: ...62 DAC 510E EN BF...

Страница 71: ...ee within North America 1 203 453 4507 Fax 1 203 453 6657 Email sales defibtech com Sales reporting defibtech com Medical Device Reporting service defibtech com Service and Repair European Authorized...

Страница 72: ...64 DAC 510E EN BF...

Страница 73: ...IVE REMEDY At Defibtech LLC s sole discretion Defibtech shall have the option to repair replace or provide a credit In the event of replacement Defibtech shall have the right at its sole discretion to...

Страница 74: ...4 D499 183 This product and its accessories are manufactured and sold under license to at least one or more of the following United States patents 5 591 213 5 593 427 5 601 612 5 607 454 5 611 815 5 6...

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