MOWOOT II
usMIMA S.L.
User Manual
Version 10
Page. 15/20
_Cancellation of Warranty
The warranty of the Device will be invalidated:
(a)
For damage produced and caused by repairs
carried out by personnel not authorized by the service station of the MOWOOT II warranty, as well as
if additional parts or accessories that are not original are replaced or used.
(b)
By manipulation of
the data of the invoice, ticket of purchase or delivery note.
_Data Protection
Your data will be included in an automated file owned by
usMIMA
for further communications
regarding repairs. You may access this file in order to exercise your rights of access, rectification,
cancellation and opposition with respect to your personal data, by means of a written
communication addressed to usMIMA, S.L.
ANNEX I - CLASSIFICATIONS
Class IIa Medical Device, Standard 93/42 / EEC, Section IX, Rule 9. The protection against electric
shock is Class A and DC. Degree of protection against electric shock of type BF (Clasif CEI EN 60601-
1.). Degree of IP 21. EC 2797. The device is not protected against water penetration. The device is
not subject to sterilization. Continuous operation device. The device is not suitable for outdoor use.
ANEXO II – ESPECIFICACIONES TÉCNICAS
Treatment time
1 - 20 min
Dimensions
220 x 170 x 130 mm
Weight
1,5 kg (3,3lbs.)
Electrical Requirements
100 - 240 VAC, 50 - 60 Hz
Number of actuators
4 units
Rated Voltage
12 VDC
Set pressure
0,65 ± 0,1 bar
Maximum Frequency of Treatment
4,5 Seconds/Cycle
Minimum Frequency of Treatment
7,5 Seconds/Cycle
Transport and Storage Temperatures Range
from -20 to 70º C
Relative Humidity of Transport and Storage
10 to 93% Hr
Operating Temperature Range
+10 to +30º C
Relative Operating Humidity
30 to 85% Hr
Atmospheric operating pressure
700 to 1060 hPa
MOWOOT II Warranty
limited 2 years or 244 hours
Classification
Class IIa (93/42/CEE)
