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Hamilton-T1 Technical Specifications

Product specifications 8 páginas · 396.76 KB · PDF

Mode form	Mode name	Mode	Adult/Ped	Neonatal
Volume-targeted modes, adaptive pressure controlled	APVcmv / (S)CMV+	Breaths are volume targeted and mandatory.	✓	✓
Volume-targeted modes, adaptive pressure controlled	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

Standard: ✓ Option: O Not applicable: --

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)	✓	✓

Standard: ✓ Option: o Not available: --

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

High-pressure O2	Pressure:	2.8 to 6 bar / 41 to 87 psi
High-pressure O2	Connector:	DISS (CGA 1240) or NIST
Low-pressure O2	Pressure:	Maximum 6 bar / 87 psi
Low-pressure O2	Connector:	Quick-coupling system, compatible with Colder Products Company (CPC) PMC series
Air supply	Integrated turbine
Inspiratory outlet (To patient port)	Connector:	ISO ID15/OD22 conical
Expiratory outlet (From patient port)	Connector (on expiratory valve)	ISO ID15/OD22 conical

Electrical specifications

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}} $

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