Philips V24CT Manuale Utente
Intended Use
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Intended Use
Description
The Philips M1165/66/67/75/76/77A CMS Patient Monitoring System and the Philips M1205A
V24 and V26 Patient Monitors are network connectable bedside patient monitoring devices.
V24 and V26 Patient Monitors are network connectable bedside patient monitoring devices.
The Philips M1205A Models V24CT and V26CT may powered by either AC line power or by
battery power.
battery power.
Purpose
The Philips M1165/66/67/75/76/77A CMS Patient Monitoring System and the Philips M1205A
V24 and V26 Patient Monitors measure and display multiple physiological parameters and
waves, and generate alarms and recordings. They exchange information with compatible
devices. The Philips M1165/66/67/75/76/77A CMS Patient Monitoring System and the Philips
M1205A V24 and V26 Patient Monitors are not therapeutic devices.
V24 and V26 Patient Monitors measure and display multiple physiological parameters and
waves, and generate alarms and recordings. They exchange information with compatible
devices. The Philips M1165/66/67/75/76/77A CMS Patient Monitoring System and the Philips
M1205A V24 and V26 Patient Monitors are not therapeutic devices.
Environment
The Philips M1165/66/67/75/76/77A CMS Patient Monitoring System and the Philips M1205A
V24 and V26 Patient Monitors are intended to be used in a clinical environment by trained
healthcare professionals. They are not intended for home use.
V24 and V26 Patient Monitors are intended to be used in a clinical environment by trained
healthcare professionals. They are not intended for home use.
They communicate with devices such as a central station through network interface ports and
a serial I/O port.
a serial I/O port.
The Philips M1165/66/67/75/76/77A CMS Patient Monitoring System and the Philips M1205A
V24 and V26 Patient Monitors are prescription devices and will carry the following label,
“United States Federal law restricts this device to sale by or on the order of a physician.”
V24 and V26 Patient Monitors are prescription devices and will carry the following label,
“United States Federal law restricts this device to sale by or on the order of a physician.”