Pari eFlow Rapid 178G1005, Instructions For Use Manual

Page: 54 / 260

50 eFlow
®
rapid - 04/18
9
TECHNICAL DATA
General
Technical electromagnetic compatibility data is available in table form upon request
from PARI Pharma GmbH or on the Internet at https://www.pari.com/fileadmin/
Electromagnetic-compatibility-4.pdf.
Classification according to DIN EN 60601-1
Electrical connection Power adapter (REF 078B7114,
Type: FW8002M/12):
Input: 100 V to 240 V~, 50-60 Hz
Output: 12 V
Batteries 4 x 1.5 V Mignon (AA LR6/Alkaline)
Rechargeable batteries 4 x 1.2 V Mignon (AA rechargeable, at
least 2100 mAh)
Nebuliser handset weight approx. 55 g
Weight eFlow
®
rapid (incl. batteries) approx. 300 g
Nebuliser handset dimensions (W x H x D) 5.0 cm x 6.3 cm x 14.5 cm
Controller housing dimensions: H 4.0 cm, Ø 11.6 cm
Min. fill volume 2.0 ml
Max. fill volume 6.0 ml
TOR (Total Output Rate)
a)
a) Measurement by laser diffraction (Helos Sympa-Tec) at 23 °C and 50% relative humidity.
Nebulised medium: 0.9% NaCl (4 ml). Inspiratory flow: 20 l/min.
610 mg/min
b)
b) May vary depending on medication and the aerosol head used.
MMD (Mass Median Diameter)
a)
4.1 μ m
b)
RF (mass fraction) < 5 μ m
a)
69%
b)
Type of electric shock protection (power adapter) Protection class II
Degree of protection from electric shock of applied part
(nebuliser handset) Type BF
Degree of protection against ingress of water as per
DIN EN 60529 (IP rating) IP 21
Degree of protection when used in the presence of
flammable mixtures of anaesthetics with air, with
oxygen or with nitrous oxide No protection
Operating mode Continuous operation