مشخصات فنی
- کپنوگراف دیجیتال با قابلیت اتصال سنسورهای Mainstream یا Microstream به انتخاب کاربر
- قابلیت تغییر واحد اندازهگیری EtCO2 به صورت mmHg، KPA و %
- ﺗﻨﻈﯿﻤﺎﺕ ﻣﺨﺼﻮﺹ ﺑﯿﻤﺎﺭﺍﻥ ﺩﺭ ﺳﻪ ﺑﺎﺯﻩ ﺳﻨﯽ: ﺑﺰﺭﮔﺴﺎﻝ، کودک ﻭ نوزاد به همراه رابط تنفسی تخصصی
- حذف عامل تداخل با سایر گازهای بیهوشی
- اندازهگیری اتوماتیک فشار محیط (اتمسفر) جهت افزایش دقت اندازهگیری EtCO2
- قابلیت افزودن ماژولهای علائم حیاتی
- ﺛﺒﺖ ﻭ ﺫﺧﯿﺮﻩﺳﺎﺯﯼ ﻓﺎﮐﺘﻮﺭﻫﺎﯼ ﺍﻧﺪﺍﺯﻩﮔﯿﺮﯼ شده (Trend)
- ﺍﺗﺼﺎﻝ ﺑﻪ شبکه ﺍﺯ ﻃﺮﯾﻖ درگاه Ethernetمطابق با پروتکل HL7
- ﺍﺗﺼﺎﻝ ﺑﻪ کامپیوتر ﺍﺯ ﻃﺮﯾﻖ درگاه USBبه همراه نرمافزار مرتبط
- ﺑﺎﻃﺮﯼ ﺩﺍﺧﻠﯽ ﺑﺎ ﻇﺮﻓﯿﺖ 5 ﺳﺎﻋﺖ ﮐﺎﺭ ﻣﺪﺍﻭﻡ
- ﺩﺍﺭﺍﯼ ﺻﻔﺤﻪ ﻧﻤﺎﯾﺶ 7/8 اینچی ﻟﻤﺴﯽ خازنی عریض
- آلارمهاي صوتي و تصويري با اولويتهاي بالا و متوسط مطابق با استاندارد IEC
- ﺗﺎﯾﯿﺪ ﺷﺪﻩ ﺗﻮﺳﻂ ﺍﺩﺍﺭﻩ ﮐﻞ ﺗﺠﻬﯿﺰﺍﺕ ﭘﺰﺷﮑﯽ ﺳﺎﺯﻣﺎﻥ ﻏﺬﺍ ﻭ ﺩﺍﺭﻭ
Technical Specification
- Internal Rechargeable Battery with 5 Hours Working Capacity
- ETHERNET Connection Complying HL7 Protocols
- USB Connector
- Unlimited Trend for Several Patients
- 7.8 inch TFT LCD with CAPACITIVE TOUCH panel
- Capability to Install other Vital Sign Modules
- Auto-Rotate Sensor for Detecting Horizontal or Vertical Positions of Display
| مشخصات الکتریکی | |
|---|---|
| Power Requirement | 80~264 VAC |
| Frequency Range | 47~63 Hz |
| Rated Power | 45 W |
| Fuse | 2 × 500 mA/250 VAC, 5 × 20 mm |
| مشخصات فیزیکی | |
|---|---|
| Dimensions (W x H x D) | 25 × 8 × 22 cm |
| Weight | 1 Kg |
| صفحهنمایش | |
|---|---|
| نوع | TFT Liquid Crystal Display (LCD),
400 × 1280 pixels, 7.8 inches |
| داده های قابل نمایش | EtCO2, Respiration Rate, FiCO2, Capnography Waveform, Alarms and Status Messages |
| باطری داخلی | |
|---|---|
| نوع | Li-Ion 7.4 V, Rechargeable, Maximum Protection |
| مدت زمان استفاده | 5 ساعت |
| مدت زمان شارژ | 3 ساعت |
| مشخصات سنسورها | ||
| Transducer Type | CAPNOSTAT® 5: Mainstream
LoFlo®: Microstream |
|
| Principle of Operation | Non-dispersive infrared (NDIR) single beam optics, dual wavelength, no moving parts | |
| Initialization Time | Less than 15 seconds for CAPNOSTAT® 5 and less than 20 seconds for LoFlo® at an ambient temperature of 25°C, full specifications within 2 minutes | |
| CO2 Measurement Range | 0 to 150 mmHg
0 to 19.7% 0 to 20 KPA (at 760 mmHg) |
|
| CO2 Rise Time | Less than 60 msec | |
| CO2 Resolution | 0.1 mmHg 0 to 69 mmHg
0.25 mmHg 70 to 150 mmHg |
|
| CO2 Accuracy (Temperature at 35° C) | 0 – 40 mmHg ± 2 mmHg
41 – 70 mmHg ± 5% of reading 71 – 100 mmHg ± 8% of reading 101 – 150 mmHg ± 10% of reading |
|
| CO2 Stability | Short Term Drift: Drift over four hours shall not exceed 0.8 mmHg maximum.
Long Term Drift: Accuracy specification will be maintained over a 120-hour period. |
|
| CO2 Noise | RMS noise of the sensor shall be less than or equal to 0.25 mmHg at 7.5% CO2 for CAPNOSTAT® 5 and at 5% for LoFlo®. | |
| Respiration Rate | Range: 0 to 150 respirations per minute (RPM) | |
| Respiration Rate Accuracy | ± 1 breath | |
| Inspired CO2 Measurement | Range: 3 to 50 mmHg | |
| Calibration | No routine user calibration required. An airway adapter zero is required when changing to a different style of airway adapter. | |
| Compensations | Expired O2, balance gas (N2, N2O, He) and anesthetic agents | |
| Total Pressure
(Barometric plus Airway pressure) |
Range: 400-850 mmHg | |
| Cross-sensitivity Compensation Error | 0-40 mmHg: ± 1 mmHg additional error
41-70 mmHg: ± 2.5% additional error 71-100 mmHg: ± 4% additional error 101-150 mmHg: ± 5% additional error |
|
| Physical characteristics | CAPNOSTAT® 5 | Weight: 25 gr
Size (WHD): 43 × 33 × 23 mm Cable length: 3 meters |
| LoFlo® | Weight: 272.16 gr
Size (WHD): 66.0 × 38.1 × 88.9 mm Cable length: 55.88 cm |
|
| لیست استانداردهای مرتبط | |
| Medical electrical equipment – Part 1: General requirements for basic safety and essential performance | IEC 60601-1:2024 |
| Medical electrical equipment – Part 1-2: General requirements for safety – Collateral standard: Electromagnetic compatibility – Requirements and tests | IEC 60601-1-2:2014 |
| Medical electrical equipment – Part 1-8: General requirements for safety – Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems | IEC 60601-1-8:2006 |
| Medical electrical equipment – Part 2-61: Particular requirements for the basic safety and essential performance of respiratory gas monitors | ISO 80601-2-61:2018 |
| Medical device software – Software life cycle processes | IEC 62304:2006 |
| Medical devices – Application of risk management to medical devices | ISO 14971:2019 |