Vapotherm 2000i, Руководство по эксплуатации

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Section 10 Warranty
Vapotherm, Inc warrants that the Vapotherm™ 2000i shall be free of defects of workmanship and
materials and will perform in accordance with the product specifications for a period of one year from
the date of sale by Vapotherm, Inc. If the product fails to perform in accordance with the product
specifications, Vapotherm, Inc. will repair, or replace, at its option, the defective materials or part. This
warranty does not cover damage caused by accident, misuse, abuse, alteration and other defects not
related to material or workmanship.
VAPOTHERM, INC. DISCLAIMS ALL LIABILITY FOR ECONOMIC LOSS, LOSS OR PROFITS, OVERHEAD OR
CONSEQUENTIAL DAMAGES WHICH MAY BE CLAIMED TO ARISE FROM ANY SALE OR USE OF THIS
PRODUCT. THIS WARRANTY IS GIVEN IN LIEU OF ALL OTHER EXPRESS WARRANTIES.
Operating Instruction Manual Page 23 Operating Instruction Manual Page 22
Attention
Consult Manual
Silence
Alarms Power
On/Off
Alternating
Current
T ype B F
Class 1
Single
Patient Use
9.2 Definitions and symbols
0297
Section 9 General Information
9.1 Specifications
Dimensions: Height 11” (280 mm), width 5.5” (140 mm), depth 4.5”
(114 mm) excluding IV pole clamp.
Weight: Less than 6 lbs (2.7 kg) without water reservoir.
Vapotherm spike set: Works with sterile water bags up to 2000 ml bag.
Circulating water volume <100 ml. (excluding Patient Patient Delivery Tube).
Mounting: Rear mounted clamp fits standard IV pole or hanger.
Power: (US) 115 V, 60 Hz, 250 VA (warm up), approximately 80 VA (continuous).
(Other versions) 220 –240 V, 5 0–60 Hz, 250 VA (warm up),
approximately 80 VA (continuous).
Gas source pressure:
4–50 psi. At high pressures (e.g. hospital wall system) the Vapotherm 2000i
must be connected to the gas outlet via a standard medical flowmeter and
flow regulator with approved fittings.
Gas flow: Controlled by external flowmeter. Operating range 1 – 40 lpm, dependent
on cartridge type and patient interface used.
Output gas temperature: (US) 33 – 43ºC at outlet of the delivery tube, adjustable by front panel
settings. (Other versions) 33 – 41ºC.
Humidification:
Vapor phase, by transpiration through microporous membrane. Output
is at least 95% relative humidity at nasal cannula at a flow rate up to
20 lpm, at least 90% at flow rates from 20 – 40 lpm, over the full range
of operating conditions.