Monitor a semnelor vitale, conceput pentru secții de spitalizare, triaj, ambulator sau verificări rapide

Va rugam sa indicati ca aceste monitoare trebuie sa fie compatibile cu statia de monitorizare centrala de Mindray. Physical Specifications Dimension: 10.8" (H) x 7.3" (W) x 5.3 (D)"27.5 cm (H) x 18.5 cm (W) x 13.5 cm (D) Weight: 7.5 lbs (3.4 kg) (with Masimo SpO2, NIBP, recorder, and a battery; without accessories.) Screen: 10.1-inch, 1280 x 800 pixels standard capacitive touchscreen support multi-touch operation TrueBP™ NIBP Meet standards of ISO 80601-2-30. Technique: Oscillometry, support inflation and deflation Operation Mode: Manual, Auto, STAT, Sequence, and BP averaging Parameters: Systolic, Diastolic, MeanTypical Measurement Time: ≤ 15 s (Inflation algorithm, with CM1303/ CM1503 cuff, PR within 60 to 200 bpm and systolic pressure within 80 to 120 mmHg)Max Measurement Time: Adult/Pediatric: 180 s, Neonate: 90 sSystolic Range: Adult: 25 to 290 mmHgPediatric: 25 to 240 mmHgNeonate: 25 to 140 mmHgDiastolic Range: Adult: 10 to 250 mmHgPediatric: 10 to 200 mmHgNeonate: 10 to 115 mmHgMean Range: Adult: 15 to 260 mmHgPediatric: 15 to 215 mmHgNeonate: 15 to 125 mmHgAccuracy: Max mean error: ± 5 mmHgMax standard deviation: 8 mmHgNIBP Resolution: 1 mmHgAssisting Venous Puncture: YesSpO2Meet standards of ISO 80601-2-61.Module: Masimo, NellcorRange Nellcor: 0 to 100%Masimo: 1 to 100%Resolution: 1%AccuracyNellcor: ±2 % (70 to 100%, Adult/Pediatric:)±3 % (70 to 100%, Neonate)Unspecified (0 to 69%)Masimo: ±2 % (70 to 100%, Adult/Pediatric, non-motion)±3 % (70 to 100%, Neonate, non-motion)±3 % (70 to 100%, motion)Unspecified (1 to 69%)Perfusion Indicator (PI) Yes, for Masimo SpO2Pitch Tone: YesRefresh Rate: ≤ 1 sPRPR Range: 20 to 300 bpm (from Nellcor SpO2) 25 to 240 bpm (from Masimo SpO2) 30 to 300 bpm (from NIBP)Accuracy: ±3 bpm (20 to 250 bpm, from Nellcor SpO2) ±3 bpm (non-motion, from Masimo SpO2) ±5 bpm (motion, from Masimo SpO2) ±3 bpm or ±3 %, whichever is greater (from NIBP)Refreshing Rate: ≤ 1 sSmarTemp™ TemperatureMeet standard of ISO 80601-2-56.Technique: Thermal resistanceOperating Mode: Predictive mode, Monitor modeTemp RangePredictive Mode: 34 to 43 °C (93.2 to 109.4 °F)Monitor Mode: 25 to 44 °C (77 to 111.2 °F)Temp Accuracy (Monitor Mode) 25 to 32 °C (not including 32 °C): ± 0.2 °C32 to 44 °C (including 32 °C): ± 0.1 °Cor 77 to 89.6 °F (not including 89.6 °F): ± 0.4 °F89.6 to 111.2 °F (including 89.6 °F): ± 0.2 °FTemp Resolution: 0.1 °CExergen TemporalScanner™ ThermometerTemp Range: 15.5°C to 42.0 °C (60.0°F to 107.6°F)Temp Accuracy: ±0.2 °C or ± 0.4 °FTemp Resolution: 0.1 °C or 0.1 °FCO2Meet standard of ISO 80601-2-55.Technique Infrared absorptionSample flow Rate: 50 ml/min (With Oridion Sampling line)Sample Flow Rate Tolerance:±15 ml/min or ±15 %, whichever is greater.Response Time: ≤ 5.0 s With an Oridion standard sampling lineSweep Speed: 3 mm/s, 6.25 mm/s, 12.5 mm/s, 25 mm/s, 50 mm/sCO2 Range: 0-150 mmHgCO2 AccuracyFull Accuracy Mode: 0 - 40 mmHg: ± 2 mmHg41 - 76 mmHg: ± 5% of reading77 - 99 mmHg: ± 10% of reading100 to 150 mmHg: ± (3mmHg + 8% of reading)ISO Accuracy Mode: Add ±2 mmHg to the full accuracy modeCO2 Resolution: 1 mmHgawRR Range: 0 to 150 rpmawRR Accuracy: ±1 rpm (0 to 59 rpm)±2 rpm (60 to 150 rpm)Apnea Time: 10 s, 15 s, 20 s, 25 s, 30 s, 35 s, 40 sManual InputSupport up to 30 manual input parameters (customizable)VS 9Page 1 of 2VITAL SIGN MONITORTechnical Specifications VS 9VITAL SIGN MONITORTechnical SpecificationsData ReviewTrends DataSpot Check Mode: Up to 5000 groupsContinuous Mode: Up to 240 hours @ 30 secondsEvents: Up to 200 eventsAlarmsAudible Indicator: 3 different alarm tones, and prompt toneVisible Indicator : Red/yellow/cyan LED, and alarm message displayProvide AlarmSight infographic alarm indicator.Clinical Assistive Application (CAA):MEWS, GCS, Pain score, Targeted Goal View, ''' Orthostatic BP Measurement '''.Blue ToothProtocol: Bluetooth 5Modulation Mode: GFSKOperating Frequency: 2402 MHz to 2480 MHzWireless Data Rate: 2 Mbps, 1 Mbps, 125 kbpsOutput Power: ≤ 8 dBm ± 4 dBData Security: AES128Wi-Fi CommunicationsProtocol: IEEE 802.11a/b/g/n/acModulation Mode: BPSK, QPSK, 16QAM, 64QAM, 256QAMOperating Frequency: 2412 MHz to 2472 MHz5180 MHz to 5320 MHz5500 MHz to 5700 MHz5745 MHz to 5825 MHzWireless Baud Rate: IEEE 802.11a: 6 to 54 MbpsIEEE 802.11b: 1 to 11 MbpsIEEE 802.11g: 6 to 54 MbpsIEEE 802.11n: MCS0 to MCS7IEEE 802.11ac: MCS0 to MCS8Output Power: < 20 dBm (CE requirement: detection mode- RMS)< 30 dBm (FCC requirement: detection mode- peak power)Operating Mode: InfrastructureData SecurityStandard: WPA/WPA2-PSK, WPA/WPA2-Enterprise, WPA/WPA2 CCKMEAP Method: LEAP, EAP-TTLS, EAP-TLS, EAP-FAST, PEAPMsChapV2, PEAP-GTC, PEAP-TLSEncryption: TKIP and AESInterfacingMain Unit: AC power connector (1)Network connector (1), RJ45USB 2.0 connector (2)Multi-Functions connect (1)Equipotential grounding terminal (1)External battery connector (1)Barcode Scanner: Support 1D and 2D barcodeThermal Recorder: 3 traces (paper 50 mm width, 20 m length)Data Output: HL7, eGateway, VitalsLink (Cerner™)Auth. Management: MLDAP, Imprivata™PowerLine Voltage: 100 to 240 VAC (±10 %)Current: 0.9 to 0.5AFrequency: 50/60 Hz (±3 Hz)Battery: 5600mAh rechargeable smart Li-ion batteryRun Time: At least 8 hours when powered by a new, fully-charged battery at 25 °C ±5 °C on standard configuration (SpO2 and NIBP), with SpO2 sensor connected, auto NIBP measurements at an interval of 15 minutes, and screen brightness set to factory default.Recharge Time (power off ): 4 hours to 100%Environmental requirementsTemperatureOperating: 0 to 40 °C (without CO2) 5 to 40 °C (with CO2)Storage: -20 to 60 °CHumidityOperating: 15 to 95 % (non condensing)Storage: 10 to 95 % (non condensing)BarometricOperating: 120 to 805.5 mmHg (57 to 107.4 kPa) (without CO2) 430 to 790 mmHg (57.3 to 105.3 kPa) (with CO2)Storage: 120 to 805.5 mmHg (16 to 107.4 kPa) (without CO2) 430 to 790 mmHg (57.3 to 105.3 kPa) (with CO2)

Bună ziua. În specificația tehnică prezentată pentru monitorul de pacient este prevăzută cerința: „Regim de măsurare: secvențial, mediu, ortostatic”. Considerăm necesar să atragem atenția asupra faptului că impunerea obligatorie a existenței funcției Orthostatic BP Measurement poate limita în mod nejustificat numărul potențialilor participanți la procedura de achiziție, în cazul în care ceea ce este necesar în mod real beneficiarului nu este un anumit mod de operare software cu o denumire comercială specifică, ci obținerea unui anumit rezultat funcțional al măsurării tensiunii arteriale. De exemplu, modul Sequence (măsurare secvențială) permite efectuarea mai multor măsurători NIBP consecutive, la intervale și cu durate prestabilite, inclusiv cu modificarea poziției pacientului și obținerea valorilor tensiunii arteriale sistolice (SIS), diastolice (DIA) și medii (MAP). Aceeași funcționalitate poate fi realizată și prin alte soluții tehnice, fără a fi legată de un anumit model sau producător, cum ar fi Mindray VS-9. Prin urmare, vă solicităm să eliminați sau să modificați această cerință, întrucât formularea actuală poate limita în mod nejustificat concurența și poate favoriza anumite soluții tehnice sau producători. Vă mulțumim!