Descargar Imprimir esta página

Microlife OXY 210 Manual De Instrucciones página 9

Ocultar thumbs Ver también para OXY 210:

Publicidad

Idiomas disponibles
  • MX

Idiomas disponibles

  • MEXICANO, página 10
Alert range:
Upper limit: 50 – 100%
Oxygen saturation:
Lower limit: 50 – 100%
Pulse rate:
Upper limit: 25 – 250 bpm
Lower limit: 25 – 250 bpm
Alert error:
Oxygen saturation: ± 1% of the
preset value
Pulse rate: the greater of ± 10%
of the preset value and ± 5 bpm
PI (Perfusion Index)
Weak PI Min. 0.2 %
Operating
5 – 40 °C / 41 – 104 °F
conditions:
15 – 80% relative
maximum humidity
Storage
-10 – +50°C / 14 – 122 °F
conditions:
10 – 93% relative
maximum humidity
Automatic
Automatically shut down in 10±2
switch-off:
seconds, when no or low signal is
detected.
Battery:
2 x 1.5 V alkaline batteries;
size AAA
Battery
approx. 30 hours
lifetime:
(using new batteries)
Microlife OXY 210
Weight:
42.5 g (including batteries)
Dimensions:
62 x 37 x 32 mm
IP Class:
IP22
Reference to
EN ISO10993-1/-5/-10;
standards:
IEC 60601-1; EN 60601-1-2;
ISO 80601-2-61; EN 62304;
EN 60601-1-6
Expected
5 years (when used 15 times/day;
service life:
20 minutes for each measurement)
Technical alterations reserved.
Note 1: The fingertip pulse oximeter measurements are
statistically distributed, only about two-thirds of pulse oxim-
eter equipment measurements can be expected to fall
within ±2% A
(Average-root-mean-square-error) of the
rmse
value measured by a co-oximeter.
Note 2: The statistic conclusion of a controlled desatura-
tion study which is guided by «ISO 80601-2-61, Annex EE,
guideline for evaluating and documenting SpO
in human subjects». The statistic result displayed the accu-
racy distribution between the range of 70% – 100%, which
is 2.83%.
Any serious incident that has occurred in relation to the
device shall be reported to the manufacturer and the
competent authority of the Member State in which the user
and / or the patient is established.
The device is a Class IIa medical device. Device complies
with European Regulation on medical devices EU MDR
2017/745.
accuracy
2
7
EN

Publicidad

loading