AED ( Automatic External Defibrillator) Physio Control

PT Dharma Bhakti Medika Sejati adalah distributor resmi di Indonesia dari Defibrillator merk Physio Control. Defibrillator Lifepak CR Plus AED dengan fitur canggih yang terpercaya dan No 1 di USA dan penjuru dunia, terpercaya dipakai untuk Emergency Basic Life Support ( BLS atau BHD) . Sangat cocok untuk dipakai di pertambangan, perminyakan, pemadam kebakaran, stasiun, terminal, bandara, pasar, mal, IGD/ UGD, ambulance. Lifepak CR Plus AED bisa dipakai oleh orang awam sekalipun karena sudah ada petunjuk pemakaian dan voice guide pada saat mesin dinyalakan. Energi shock dari 0 - 360 Joule dan BiPhasic ( tidak mengakibatkan kerusakan jantung) . LifePak CR Plus AED pada saat dibuka, petunjuk suara dari mesin akan memberi guide dan ada gambar juga pada setiap electrode pad nya untuk dipasang disebelah mana pada anatomi tubuh. LifePak CR Plus AED akan memberikan energi secara otomatis sebesar sesuai yang diperlukan oleh tubuh pasien. Pada saat pasien membutuhkan CPR maka mesin suara otomatis akan memberi tahu kepada penolong/ paramedic untuk melakukan CPR. Dan setelah dilakukan CPR berdasarkan AHA ( 30: 2 atau 100/ min terus menerus) maka mesin LifePak CR Plus AED akan menganalisa apakah pasien masih memerlukan bantuan kejut jantung lagi. Jika kondisi pasien sudah stabil, mesin akan menganalisa otomatis dan memberi petunjuk tidak memerlukan shock/ kejut jantung lagi. Tersedia juga AED CR Plus Trainer untuk keperluan BLS/ ACLS Training. Paket ini sudah termasuk Ambu Rescue Mask dan carrying case ( tas) Spesifikasi secara lengkap bisa di lihat di situs kami www.ptdbms.com Specification Waveform : Adaptiv Biphasic truncated exponential, with voltage and current duration compensation for patient impedance. Output Energy Sequence : Multiple levels, configurable from 150 joules to 360 joules Output Energy Accuracy : ± 10% into 50 ohms, ± 15% into 25 to 100 ohms. Shock Advisory System : Shock Advisory System: An FCG analysis System that advises whether a shock is appropriate; meets rhythm recognition criteria specified in DF39 The device allows for a defibrillation shock only if the Shock Advisory System advises defibrillation. Device Capacity Typical : Thirty ( 30) full discharges or 210 minutes of " on time" with a fully charged device. Minimum : Twenty ( 20) full discharges or 140 minutes of " on time" with a fully charged device. Shock Charge Time : Charge times with a fully charged device : 200 joules in less than 9 seconds, 360 joules in less than 15 seconds. System Recharge Times : Recharge times with a fully discharged device: Able to deliver 6 shocks or provide 42 minutes of operating time after 24 hours of recharge time and 20 shocks or 140 minutes of operating lime after 72 hours of recharge time with a new CHARGE-PAK at temperatures above 15° C { 59° F) . Controls : Lid Release/ ON-OFF - Controls device power. After electrodes are attached to a patient, the fully automatic version of the device deliver a shock, if appropriate, not requiring operator intervention. Electrical Protection : Input protected against high voltage defibrillator pulses per IEC60601-1/ EN60601 -1 Safety Classification : Internally powered equipment. IEC60601-1/ EN60601-1. FDA approval User Interface User Interface : The user interface includes voice instructions, audible tones and graphical prompts. Readiness Display : The readiness display shows the device status. OK Indicator : Shows OK when the last self-test was completed successfully. When the OK indicator is visible, all other indicators are not visible. The OK indicator is not displayed during device operation. Self Test : Battery, pads ( presence and function) , internal electronics, shock button, software CHARGE-PAK Indicator : When displayed, replace the CHARGE-PAK battery charger and electrode pads. Attention Indicator : When first displayed, at least six ( 6) discharges or 42 minutes of operating time remain. Service Indicator : Service required when displayed. Environmental Note : All performance specifications defined assume the unit has been stored ( two hours minimum) at operating temperature prior to operation Operating Temperature : 0° to + 50° C ( + 32° to + 122° F) . Storage Temperature : -40° to + 70° C ( -40° to + 158° F) with CHARGE-PAK charger and : electrodes, maximum exposure time limited to one week. Atmospheric Pressure : 760 mmHg to 429 mmHg, 0 to 15, 000 feet above sea level. Relative Humidity : 5 to 95% ( non-condensing) . Water Resistance : IEC60529/ EN60529 IPX4 " Splash proof" with electrodes connected CHARGE-PAK installed. Shock : MIL-STD-810E, Method 516.4, Procedure 1, ( 40g, 6-9 ms pulse, ½ sine each axis) . Vibration : MIL-STD-810E, Method 514.4, Helicopter - category 6 ( 3.75 g rms) and Ground Mobile - category 8 ( 2.85 g rms) . Physical characteristic Height : 10.7 cm ( 4.2 in) Width : 20.3 cm ( 8.0 in) Depth : 24.1 cm ( 9.5 in) , excluding handle Weight : 2.0 kg ( 4.5 lbs) with CHARGE-PAK and electrodes Default Settings Energy Sequence Energy sequence is set to 200J, 300J, 360J Motion Detection The motion detection system is set to on during analysis Energy Protocol The energy protocol is set to increase energy only after a lower energy shock was unsuccessful Stack Shocks Stack shocks option is set to off Turn-On Prompt The turn-on prompt is set to provide voice prompts upon power on CPR Time The CPR Time is set to 120 seconds. Voice Prompt Volume The voice prompt volume is set to high. Accessories CHARGE-PAK Battery Charger Type : Li/ SO2Cl2 Lithium Sulfuryl Chloride, 11.7V, 1.4 amp-hours. Replacement: : Replace the CHARGE-PAK battery charger and QUIK-PAK™ electrodes packet after using the defibrillator, if the CHARGE-PAK symbol appears in the readiness display or when the Use By date is reached ( typically 2 years) . Weight: : 80.5 grams ( 0.18 lb) QUIK-PAK Electrode Pads Pads : ECG is received from disposable defibrillation electrodes, standard placement ( anterior-lateral) Pads Packaging : User intuitive, rapid release QUIK-PAK electrodes allow the electrode pads to be preconnected to the device and protected under a top cover. Pads Replacement: : Replace every two ( 2) years Infant/ Child Reduced Energy : For use on infants and children less than 8 years of age or less than 55 lbs ( 25kg) . Data storage Memory Type : Internal digital memory. ECG Storage : Dual patient data storage. Minimum 20 minutes of ECG stored for the current patient, summarized data stored for the previous patient. Report Types : ð Continuous ECG - A continuous patient ECG report. : ð Summary - A summary of critical resuscitation events and ECG waveform segments associated with these events. : ð Event log report - A report of time stamped markers, which reflect operator and device activity. : ð Test log report - A device self-test activity report. Capacity : Minimum 200 time-stamped event log markers. Communications : Wireless transfer to a personal computer. Data Review : Physio-Control provides an array of tools lo meet customer needs for data viewing and analysis ð The specifications apply from 25 to 200 ohms, Voltage compensation is limited to the voltage that would result in delivery of 360 joules into 50 ohms. All specifications are at 20" C unless otherwise staled