11
designed to provide reasonable protection against
harmful interference in a typical medical installation.
2
Sensor LED light emissions fall within Class 1 level,
according to IEC/EN 60825-1:2001. No special safety
precautions are required.
3
Normal operation means:
The oximeter is turned on;
A sensor is connected to the oximeter;
The sensor is applied to the patient;
The patient’s SpO2, Pulse rate are being
reported;
No error conditions exist.
4
Wash the probe with clean water after disinfecting it to
remove any remaining solution. The probe can only be
reused after dried thoroughly.
5
Do not disinfect the probe with the water boiled.
6
Any residue should be removed from the probe before
being disinfected, and avoid contacting corrosive
solvent. Dipping the cable into alcohol or alkalescent
solvent for a long time may reduce the flexibility of the
scarfskin of the cable. Also, the connector should not be
dipped.
7
After monitoring, disinfect the probe according to the
instruction described in the user manual.
8
The materials with which the patient or any other person
can come into contact conform with the standard of
ISO10993.
9
The pictures and interfaces in this manual are for
reference only.
10
A functional tester cannot be used to assess the
accuracy of the oximeter probe or the oximeter.
11
The operating time of the Ni-MH rechargeable battery
package depends on the configuration and operation of
the pulse oximeter.
Summary of Contents for HS-Vet
Page 1: ......
Page 65: ...64 Appendix Ⅲ Record Table ID No Name Time SpO2 PR NOTE ...
Page 98: ...97 Configuración del sistema Configuración de alarma ...
Page 136: ...135 pulsioxímetro ...
Page 139: ...138 Apéndice III Tabla de registro Nº ID Nombre Hora SpO2 PR NOTA ...
Page 204: ...203 Annexe Ⅲ Record Table No ID Nom Temps SpO2 PR REMARQUE ...
Page 237: ...236 Alarm Setup ...
Page 278: ...277 Anhang III Tabelle für Aufzeichnungen ID Nr Bezeichnung Zeit SpO2 PF HINWEIS ...