Cleaning And Disposal; Technical Data; Order List - Dräger VentStar heated Instrucciones De Uso

WARNING
Risk of patient injury
Interchanging the inspiratory hose with the temperature sensor
ports and the expiratory hose in the dual heated breathing circuit
endangers the patient.
The temperature sensor ports must be located in the inspiratory
limb of the dual heated breathing circuit.
CAUTION
Risk of patient injury
Too high or too low ambient temperatures can lead to increased
accumulation of humidity or humidification performance can be
reduced.
Do not operate the device outside the stated ambient temperature
range.
NOTE
This medical device has been designed, tested, and manufactured
exclusively for single-patient use and for a period of use not exceeding
7 days.

Cleaning and disposal

The user is responsible for regularly replacing the medical device
according to the hygiene regulations.
WARNING
Reuse, reprocessing, or sterilization can lead to failure of the
medical device and cause injury to the patient.
This medical device has been designed, tested, and
manufactured exclusively for single use. The medical device
must not be reused, reprocessed, or sterilized.
WARNING
Following use, the medical device must be disposed of according
to local public health and waste disposal regulations in order to
avoid possible contamination.

Technical data

Breathing hose length 1,5 m (59 in)
Material
Breathing hoses PP
Connections PP
Y-piece PP
Humidifier chamber PC, SBC, silicone, aluminum
All gas-conducting components are free of PVC.
Performance data
Breathing circuit
1)
Insp./exp. resistance at 60 L/min <2.1 mbar
Insp./exp. resistance at 30 L/min <0.7 mbar / <0.5 mbar
Insp./exp. resistance at 15 L/min <0.2 mbar / <0.2 mbar
Insp./exp. resistance at 5 L/min <0.1 mbar / <0.1 mbar
Insp./exp. resistance at 2.5 L/min <0.1 mbar / <0.1 mbar
Compliance at 60 mbar <2.8 mL/mbar
Leakage at 60 mbar <50 mL/min
Electrical connection data 22 V, 2.73 A, 60 W, 16
Humidifier chamber volume 130 mL
Warm-up time 30 min
Humidifier output:
Invasive ventilation at 10 to 60 L/min >33 mg/L
Ambient conditions
During storage
Temperature –20 to 60 °C (–4 to 140 °F)
Relative humidity 5 % to 95 % (non-condensing)
Atmospheric pressure 500 to 1200 hPa (7.3 psi to
17.4 psi)
During operation
Temperature 18 to 26 °C (64 to 79 °F)
Relative humidity 5 % to 95 % (non-condensing)
Atmospheric pressure 500 to 1200 hPa (7.3 psi to
17.4 psi)
Classification according to Directive Class IIa
93/42/EEC Annex IX
UMDNS code 14-238
Universal Medical Device
Nomenclature System –
nomenclature for medical devices
Protection class I, Type BF
1) 1 bar = 1 kPa x 100
2) 1 mbar = 1 cmH O
2

Order list

Designation
For adult use:
VentStar dual heated
VentStar heated
For neonatal patients:
VentStar heated (N)
VentStar heated (N) Basic
VentStar humidifier chamber
Additional items according to Dräger accessories
catalog
Instructions for use VentStar heated and VentStar dual heated
2)
/ <1.6 mbar
Ω
Part no.
MP00306
MP00307
MP00308
MP00309
MP00234
English
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