Technical Data; General; Classification According To Din En 60601-1 - Pari eFlow rapid Manual Del Usuario

TECHNICAL DATA

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General

Electrical connection
Batteries
Rechargeable batteries
Nebuliser handset weight
®
Weight eFlow rapid (incl. batteries)
Nebuliser handset dimensions (W x H x D)
Control unit housing dimensions
Min. fill volume
Max. fill volume
TOR (Total Output Rate)
MMD (Mass Median Diameter)
RF (Mass fractions) < 5 μm
a) Measurement using laser diffraction (Helos SympaTec) at 23 °C and 50% relative humidity. Nebulised
medium: 0.9% NaCl (4 ml). Inspiratory flow: 20 l/min.
b) May vary depending on medication and the aerosol head used.
Technical electromagnetic compatibility data is available in table form upon request
from PARI Pharma GmbH or on the Internet at www.eflowrapid.info.

Classification according to DIN EN 60601-1

Type of electric shock protection (power adapter)
Degree of protection from electric shock of part used
(nebuliser)
Degree of protection against ingress of water as per
DIN EN 60529 (IP rating)
Degree of protection when used in the presence of
flammable mixtures of anaesthetics with air, with
oxygen or with nitrous oxide
Operating mode
®
eFlow rapid - 01/17
a)
a)
a)
Power adapter (REF 078B7106,
Type FW7555M/12):
Input: 100 V - 240 V~, 50/60 Hz
Output: 12 V
4 x 1.5 V Mignon (AA LR6/Alkaline)
4 x 1.2 V Mignon (AA rechargeable,
at least 2100 mAh)
approx. 55 g
approx. 300 g
5.0 cm x 6.3 cm x 14.5 cm
H 4.0 cm, Ø 11.6 cm
2.0 ml
6.0 ml
b)
610 mg/min
b)
4.1 μm
b)
69%
Protection class II
Type BF
IP 21
No protection
Continuous operation
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