DESIGNED FOR:
to perform temporary endocardial stimulation of one or two heart chambers in patients with heart rhythm disorders.
SPECIAL FEATURES:
determination of the quality of the electrode installation in the heart chambers without additional equipment - "intraoperative tester";
display of an electrogram for positioningthe electrode in the heart chambers without and additional equipment;
prompt determination of the possibility of undesired stimulation of phrenic nerve or pectoral muscles at high amplitude of stimulation pulses.
CAPABILITIES:
stimulation amplitude, V: 0.1- 17:
stimulation modes: S00 (A00, V00), SST (AAT, VVT), SSI (AAI, VVI), D00, VDD, DVI, DDD, emergency, relief (ultra-frequency stimulation);
base frequency, pulse/min: 30 -250;
relief frequency, pulse/min: 60 -1000;
AV-delay, ms: 15 - 400;
stimulation impulses are indicated by yellow LEDs;
detected signals of spontaneous heart activity are indicated by green LEDs;
low battery residual power is indicated by flickering red LED and an audible signal;
device weight is not more than 250 grams.
POWER SUPPLY:
power is supplied by a lithium or alkaline battery type 6F22;
stimulation time after disconnection of battery for replacement - at least 30 seconds.
Equipment is certified and approved for use