| Mode form | Mode name | Mode | Adult/Ped | Neonatal |
| Volume-targeted modes, adaptive pressure controlled | APVcmv / (S)CMV+ | Breaths are volume targeted and mandatory. | ✓ | ✓ |
| APVsimv / SIMV+ | Volume-targeted mandatory breaths can be alternated with pressure-supported spontaneous breaths. | ✓ | ✓ |
| Pressure-controlled modes | PCV+ | All breaths, whether triggered by the patient or the ventilator, are pressure-controlled and mandatory. | ✓ | ✓ |
| PSIMV+ | Mandatory breaths are pressure controlled. Mandatory breaths can be alternated with pressure-supported spontaneous breaths. | ✓ | ✓ |
| DuoPAP | Mandatory breaths are pressure controlled. Spontaneous breaths can be triggered at both pressure levels. | O | O |
| APRV | Spontaneous breaths can be continuously triggered. The pressure release between the levels contributes to ventilation. | O | O |
| SPONT | Every breath is spontaneous, with or without pressure-supported spontaneous breaths. | ✓ | ✓ |
| Intelligent ventilation | ASV | Operator sets %MinVol, PEEP, and Oxygen. Frequency, tidal volume, pressure, and I:E ratio are based on physiological input from the patient. | ✓ | -- |
| Noninvasive modes | NIV | Every breath is spontaneous. | O | O |
| NIV-ST | Every breath is spontaneous as long as the patient is breathing above the set rate. A backup rate can be set for mandatory breaths. | O | O |
| nCPAP | Demand flow Nasal Continuous Positive Airway Pressure. | -- | O |
| nCPAP-PC | Breaths are pressure controlled and mandatory. | -- | O |
| High flow oxygen therapy | HiFlowO2 | High flow oxygen therapy. No supported breaths. | O | O |
| Functions | Adult/Ped | Neonatal |
| Capnography, mainstream (volumetric) and sidestream | ○ | ○ |
| Communication ports: COM1 port, USB port, Nurse call | ○ | ○ |
| Communication protocols: for details see Connectivity brochure | ○ | ○ |
| Dynamic Lung | ✓ | -- |
| Event log (up to 1000 events with data and time stamp) | ✓ | ✓ |
| Handles for various options (jet, ambulance, or bed rail mount) | ○ | ○ |
| IntelliTrig (leak compensation) | ✓ | ✓ |
| Languages | ✓ | ✓ |
| (English, US-English, Chinese, Croatian, Czech, Danish, Dutch, Finnish, French, German, Greek, Hungarian, Indonesian, Italian, Japanese, Korean, Norwegian, Polish, Portuguese, Romanian, Russian, Serbian, Slovak, Spanish, Swedish, Turkish) | ✓ | ✓ |
| Manual breath/prolonged inspiration | ✓ | ✓ |
| NBC filter (only for HAMILTON-T1 Military) | ○ | ○ |
| Nebulization, pneumatic | ✓ | -- |
| Night Vision Goggles (NVG) option | ○ | ○ |
| O2 enrichment | ✓ | ✓ |
| Oxygen adjustable from 21% to 100% | ✓ | ✓ |
| Patient group | ✓ | ○ |
| Print screen | ✓ | ✓ |
| Screen lock | ✓ | ✓ |
| Second battery (hot-swappable) | ○ | ○ |
| Speak valve compatibility | ○ | -- |
| SpO2 monitoring | ○ | ○ |
| Standby with timer | ✓ | ✓ |
| Suctioning tool | ✓ | -- |
| Trends/Loops | ○ | ○ |
| Flow trigger | ✓ | ✓ |
| Vent Status (Visual representation of ventilator dependence) | ✓ | ✓ |
| Description | Specification |
| Automatic expiratory base flow | Adult/Ped: Fixed at 3 l/min Neonatal: Fixed at 4 l/min |
| Inspiratory pressure | 0 to 60 cm $ H_{2}O $ |
| Maximum inspiratory flow | 260 l/min (120 l/min with 100% O $ _{2} $) |
| Minimum expiratory time | 20% of cycle time; 0.2 to 0.8 seconds |
| Means of inspiratory triggering | Flow trigger control |
| Oxygen mixer accuracy | $ \pm $ (volume fraction of 2.5% + 2.5% of actual reading) |
| Preoperational checks | Tightness test, Flow Sensor/O $ _{2} $ sensor/CO $ _{2} $ sensor calibration |
| Tidal volume | Adult/Ped: 20 to 2000 ml Neonatal: 2 to 300 ml |
| Brightness setting for display | The range is 10% to 100% brightness. By default, Day is set to 80%; Night is set to 40%. |
| Brightness with NVG option | The range is 1 to 10. The default is 5. |
| Classification | Class IIb, continuously operating according to EC directive 93/42/EEC |
| Certification | IEC 60601-1:2005/A1:2012, IEC 60601-1-2:2014, ANSI/AAMI ES60601-1:2005/(R)2012, ISO 80601-2-12:2011, CAN/CSA-C22.2 No. 60601-1:14, EN ISO 5356-1:2015, ISO 80601-2-55:2011 |
| Declaration | The HAMILTON-T1 was developed in accordance with pertinent international standards and FDA guidelines. The ventilator is manufactured within an EN ISO 13485 and EN ISO 9001, Council Directive 93/42/EEC, Annex II, Article 3 certified quality management system. The ventilator meets the Essential Requirements of Council Directive 93/42/EEC, Annex I. |
| Electromagnetic compatibility | According IEC 60601-2:2014 |
| Air transport compatibility | EN1789:2007+A2:2014, EN 13718-1:2014, EN 794-1:1997 +A2:2009, RTCA/DO-160G, MIL-STD-461F, MIL-STD-810G, Chg. 1, Meth 500.6, Proc. II Operation/Air Carriage, mod. |
| Safety Class | Class II, Type B applied part (ventilator breathing system, VBS), type BF applied part CO2 sensor including CO2 module connector; SpO2 sensor including adapter, continuous operation according to IEC 60601-1 |
| Graphic type/tab name | Options |
| Waveforms | Pressure, Volume, Flow, $ PCO2^{{1}} $, $ FCO2^{{1}} $, Plethysmogram $ ^{{2}} $ |
| Intelligent panels | Dynamic Lung $ ^{{3}} $, Vent Status, ASV Graph $ ^{{4}} $ |
| Trends | 1-, 6-, 12-, 24-, or 72- $ h^{{5}} $ trend data for a selected parameter or combination of parameters |
| Loops | Pressure/Volume, Pressure/Flow, Volume/Flow, Volume/PCO2 $ ^{{1}} $, Volume/FCO2 $ ^{{1}} $ |
