dea nihon kodhen
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Introduction
OPERATORS MANUAL
Automated External DefibrillatorCardiolife
AED-2100K
Installation
General Handling
Precautions
Contents
Checking the AED
Voice Instructions
Using the AED
Reference
First Edition: 08 Oct 2008
0614-901835Printed:
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WARRANTY POLICYNihon Kohden Corporation (NKC) shall warrant its products against all defects in materials and workmanship for five years from the
date of delivery. However, consumable materials such as battery pack and defibrillation pads are excluded from the warranty.
NKC or its authorized agents will repair or replace any products which prove to be defective during the warranty period, provided
these products are used as prescribed by the operating instructions given in the operators manual.
No other party is authorized to make any warranty or assume liability for NKCs products. NKC will not recognize any other
warranty, either implied or in writing. In addition, service, technical modification or any other product change performed by someone
other than NKC or its authorized agents without prior consent of NKC may be cause for voiding this warranty.
Defective products or parts must be returned to NKC or its authorized agents, along with an explanation of the failure. Shipping costs
must be pre-paid.
This warranty does not apply to products that have been modified, disassembled, reinstalled or repaired without Nihon Kohden
approval or which have been subjected to neglect or accident, damage due to accident, fire, lightning, vandalism, water or other
casualty, improper installation or application, or on which the original identification marks have been removed.
EMC RELATED CAUTION
This equipment and/or system complies with IEC 60601-1-2 International Standard for electromagnetic
compatibility for medical electrical equipment and/or system. However, an electromagnetic environment
that exceeds the limits or levels stipulated in IEC 60601-1-2, can cause harmful interference to the
equipment and/or system or cause the equipment and/or system to fail to perform its intended function or
degrade its intended performance. Therefore, during the operation of the equipment and/or system, if there
is any undesired deviation from its intended operational performance, you must avoid, identify and resolve
the adverse electromagnetic effect before continuing to use the equipment and/or system.
The following describes some common interference sources and remedial actions:
1. Strong electromagnetic interference from a nearby emitter source such as a cellular phone:
Turn off the cellular phone.
2. Effect of direct or indirect electrostatic discharge:
Make sure all users and patients in contact with the equipment and/or system are free from direct or
indirect electrostatic energy before using it. A humid room can help lessen this problem.
3. Electromagnetic interference with any radio wave receiver such as radio or television:
If the equipment and/or system interferes with any radio wave receiver, locate the equipment and/or
system as far as possible from the radio wave receiver.
General Handling Precautions
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4. Use with other equipment:
When the equipment and/or system is adjacent to or stacked with other equipment, the equipment and/
or system may affect the other equipment. Before use, check that the equipment and/or system
operates normally with the other equipment.
5. Use of unspecied accessory, transducer and/or cable:
When an unspecied accessory, transducer and/or cable is connected to this equipment and/or system,
it may cause increased electromagnetic emission or decreased electromagnetic immunity. The
specied conguration of this equipment and/or system complies with the electromagnetic requirements
with the specied conguration. Only use this equipment and/or system with the specied conguration.
If the above suggested remedial actions do not solve the problem, consult your Nihon Kohden distributor or
representative for additional suggestions.
For EMC compliance, refer to Specifications - Electromagnetic Emissions/Immunity in the Reference section.
The CE mark is a protected conformity mark of the European Community. The products herewith comply with
the requirements of the Medical Device Directive 93/42/EEC and Radio and Telecommunications Terminal
Equipment Detective 1999/5/EC.
NOTE about Waste Electrical and Electronic Equipment (WEEE) directive 2002/96/EECFor the member states of the European Union only:
The purpose of WEEE directive 2002/96/EEC is, as a rst priority, the prevention of waste electrical and
electronic equipment (WEEE), and in addition, the reuse, recycling and other forms of recovery of such
wastes so as to reduce the disposal of waste.
Contact your Nihon Kohden representative for disposal at the end of its working life.
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:
(1) this device may not cause harmful interference, and
(2) this device must accept any interference received, including interference that may cause undesired operation.
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When the lid is closed
Explanation of Parts
Introduction
ON
OFF
Lid
Power switch
Battery pack holder
Enabled
Disabled
Status Indicator
Buzzer
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When the lid is open
Battery pack
Latch Battery connector
Front Back
Defibrillation pad holder
Diagnostics panel
Defibrillation pad connector
Shock button
Cable guides
Adult/child mode switch
Pads placement
indicator
Speaker
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AEDWhen you turn the AED power on and open the lid, the AED starts voice instructions.
When the AED determines that a defibrillation shock is required, the AED starts charging.
When charging is complete, the Shock Button flashes. When you press the Shock Button,
the AED delivers a shock. The data collected during resuscitation, such as the heart rhythm,
is recorded in the internal memory.
Battery pack (consumables)The AEDs dedicated battery pack stores important information, such as the length of
operation and remaining battery power, in the memory inside the battery pack. The battery
condition is checked by AED self test every day. If the AED is never used for resuscitation,
the battery power lasts for about two years. Since the battery pack is not rechargeable,
replace it with a new one when the battery power runs out.
p. 9 Battery Pack in the General Handling Precautions section
Defibrillation pads (consumables)One package contains two pads to be placed on the patient. Connect the pads connector to
the AED and put the package into the holder on the back of the lid. Since the pads are
disposable, replace them with new ones after use. Replace the pads if they are past the
expiration date, even if they have never been used. The expiration date is printed on the
package.
There are two types of defibrillation pads: defibrillation pads for adult and defibrillation
pads for child. If the patient is older than 8 years old, use the defibrillation pads for adult
and if the patient is a child age 1 to 7, use the defibrillation pads for child.
p. 10 Defibrillation Pads in the General Handling Precautions section
Note: Defibrillation pads are sold separately. Also read the document attached to the defibrillationpads.
Items to be CheckedMake sure that the necessary items are ready.
To order additional consumables, contact a Nihon Kohden representative.
Introduction
The illustration shows the P-531KDefibrillation Pads for Adult
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Giri
KULLANIM KILAVUZU
Otomatik Harici DefibrilatrCardiolife
AED-2100K
Montaj
Genel Kullanm
Uyarlar
indekiler
AEDnin Kontrol
Sesli Talimatlar
AEDnin Kullanm
Referans
lk Bask: 08 Ekim 2008
0614-901835Bask:
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GARANT POLTKASINihon Kohden Corporation (NKC) rnleri iin teslim tarihinden itibaren beyl malzeme ve iilik garantisi vermektedir. Ancak,batarya ve defibrilasyon pedleri gibi sarf malzemeleri bu garanti kapsamnda deildir.
NKC veya yetkili temsilcileri, sz konusu rnlerin kullan m klavuzunda verilen kullanm talimatlarna uygun kullanlmaskaydyla,
garanti sresi iinde arzalanan rnleri onaracak veya deitirecektir.
NKC rnleri iin baka hibir ahs garanti veremez veya sorumluluk stlenemez. NKC rtl veya yaz lbaka hibir garanti kabuletmeyecektir. Ayrca, NKCnin nceden onayalnmadan NKC veya yetkili temsilcileri dnda herhangi biri tarafndan servis, teknikdeiiklik veya dier rn deiiklikleri bu garantinin geersizlemesine neden olabilir.
Arzalrnler veya paralar, arzann bir aklamasyla birlikte NKC veya yetkili temsilcilerine iade edilmelidir. Nakliye giderleri
nceden denmelidir.
Bu garanti Nihon Kohdenin onayolmadan deitirilen, sklen, yeniden monte edilen veya onarlan veya ihmal veya kaza sonucuzarar gren, kaza, yangn, yldrm, fiziksel iddet, su veya ngrlemeyen baka kazalar, yanlmontaj veya uygulamalar nedeniyleoluan hasarlar veya orijinal tanmlama iaretlerinin silindii rnler iin geerli deildir.
EMC LE LGL UYARI
Bu ekipman ve/veya sistem tbbi elektrikli ekipman ve/veya sistemlerin elektromanyetik uygunluu ile ilgili
IEC 60601-1-2 Uluslararas Standardna uygundur. Bununla birlikte, IEC 60601-1-2de belirtilen limitleri
veya seviyeleri aan bir elektromanyetik ortam ekipman ve/veya sistemde zararl parazite neden olabilir ve/
veya ekipman ve/veya sistemin ngrlen fonksiyonunu yerine getirememesine veya performansnn
dmesine neden olabilir. Bu nedenle, ekipmann ve/veya sistemin kullanm srasnda, ngrlen
performansndan istenmeyen bir sapma grld takdirde, ekipman ve/veya sistemi kullanmaya devametmeden nce olumsuz elektromanyetik etkiyi tespit etmeniz ve halletmeniz gerekir.
Aada baz yaygn parazit kaynaklar ve zm nerileri belirtilmektedir:
1. Yaknlardaki cep telefonu gibi bir vericiden kaynaklanan gl bir elektromanyetik parazit:
Cep telefonunu kapatn.
2. Dorudan veya dolayl bir elektrostatik dearjn etkisi:
Kullanmaya balamadan nce, ekipmanla ve/veya sistemle temas eden tm kullanclar ve hastalar
kontrol ederek dorudan veya dolayl olarak elektrostatik enerji tamadklarndan emin olun. Nemli bir
oda bu sorunu azaltabilir.
3. Radyo veya televizyon gibi radyo dalgas alclarndan kaynaklanan elektromanyetik parazitler:
Ekipman ve/veya sistem bir radyo dalgas alcsndan etkileniyorsa, ekipman ve/veya sistemi radyo
dalgas alcsndan olabildiince uzaa yerletirin.
Genel Kullanm Uyarlar
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4. Baka ekipmanlarla kullanm:
Ekipman ve/veya sistem baka ekipmanlarn yannda veya yaknndayken, ekipman ve/veya sistem
dier ekipman etkileyebilir. Kullanmaya balamadan nce, ekipmann ve/veya sistemin dier
ekipmanlarla normal bir ekilde altndan emin olun.
5. Belirtilen aksesuarlarn, transformatrn ve/veya kablonun kullanldndan emin olun:
Bu ekipmana ve/veya sisteme belirt ilmeyen bir aksesuar, transformatr ve/veya kablo baland
takdirde, bu elektromanyetik emisyonun artmasna veya elektromanyetik bakln azalmasna neden
olabilir. Bu ekipmann ve/veya sistemin belirtilen konfigrasyonu, belirtilen konfigrasyonun
elektromanyetik gerekliliklerine uygundur. Bu ekipman ve/veya sistemi yalnzca belirtilen
konfigrasyonla kullann.
Yukarda nerilen ilemler sorunu zmedii takdirde, baka neriler iin Nihon Kohden distribtrne veya
temsilcisine bavurun.
EMC uygunluu iin, Referans blmndeki Spesifikasyonlar - Elektromanyetik Emisyonlar/Baklk balna bakn.
CE ibaresi Avrupa Topluluunun koruma altndaki bir uygunluk ibaresidir. Burada belirtilen rnler 93/42/EEC
sayl Tbbi Cihazlar Direktifine ve 1999/5/EC sayl Radyo ve Telekomnikasyon Terminal Cihazlar Direktifine
uygundur.
2002/96/EEC sayl Elektrikli ve Elektronik Ekipman Atklar (WEEE) ile ilgili NOT
Yalnzca Avrupa Birlii yesi lkeler iin:
2002/96/EEC sayl WEEE direktifinin amac, ilk ncelik olarak, elektrikli ve elektronik ekipman atklarnn
(WEEE) nlenmesi ve ayrca, daha az atk atlmasn salamak iin bu atklarn yeniden kullanlmas, geri
dntrlmesi veya baka biimlerde kurtarlmasn salamaktr.
rn kullanm mrnn sonuna geldiinde atlmasn salamak iin Nihon Kohden temsilcisine bavurun.
Bu cihaz FCC KurallarBlm 15e uygundur. Kullanmaadaki iki arta tabidir:
(1) bu cihaz zararlparazite yol aamaz, ve
(2) bu cihaz, istenmeyen almann dahil olduu parazit dahil olmak zere, maruz kaldtm parazitleri tolere etmelidir.
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Kapak kapalyken
Paralarn Aklamalar
Giri
AIK
KAPALI
Kapak
G anahtar
Batarya yuvas
Etkinletirildi
Devreden karld
Durum Gstergesi
Zil
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Kapak akken
Batarya
Mandal Batarya konektr
n Arka
Defibrilasyon pedi yuvas
Tanlama paneli
Defibrilasyon pedi konektr
ok dmesi
Kablo klavuzlar
Yetikin/ocuk modu anahtar
Ped yerletirme
gstergesi
Hoparlr
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AEDAEDnin gcn atnzda ve kapanatnzda, AED sesli talimatlara balar. AED bir
defibrilasyon okunun gerekli olduunu belirlediinde, arj olmaya balar. arj
tamamlandnda, ok Dmesi yanp snmeye balar. ok Dmesine bastnzda, AED
bir ok verir. Ressitasyon srasnda toplanan kalp ritmi gibi veriler dahili bellekte saklan r.
Batarya (sarf malzemeleri)AEDnin zel batarya paketinde, operasyonun sresi ve kalan pil arjgibi nemli bilgiler
bataryann iindeki bellekte saklanr. Bataryann durumu her gn AEDnin z snamas
srasnda test edilir. AED ressitasyon iin hi kullan lmadtakdirde, batarya yaklak iki
yl dayanabilir. Batarya yeniden doldurulabilir olmadiin, gc tkenen bataryay
yenisiyle deitirin.
s.9 Genel Kullanm Uyarlar blmnde Pil mr bal
Defibrilasyon pedleri (sarf malzemeleri)Bir pakette hastaya yerletirilecek iki ped bulunur. Pedlerin konektrn AEDe balayn
ve paketi kapan arkasndaki yuvaya koyun. Pedler tek kullanmlk olduu iin,
kullandktan sonra yenileriyle deitirin. Son kullanm tarihi geen pedleri, hi
kullanlmamolsalar bile deitirin. Son kullanm tarihi paketin arkasnda basldr.
ki tip defibrilasyon pedi vardr; yetikin defibrilasyon pedleri ve ocuk defibrilasyon
pedleri. Hasta 8 yandan bykse, yetikin defibrilasyon pedlerini, hasta 1 ile 7 ya
arasnda bir ocuksa ocuk defibrilasyon pedlerini kullann.
s.9 Genel Kullanm Uyarlar blmnde Defibrilasyon Pedleri bal
Not: Defibrilasyon pedleri ayrca satlr. Ayrca defibrilasyon pedleri ile birlikte gelen belgeyide okuyun.
Kontrol Edilmesi Gereken elerGerekli elerin hazr olduundan emin olun.
lave sarf malzemesi siparii vermek iin, bir Nihon Kohden temsilcisine bavurun.
Giri
Resimde Yetikinler iin P-531KDefibrilasyon Pedleri gsterilmektedir.
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