Datascope - CS300
by Datascope
Datascope - CS300
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DESCRIPTION
The New CS300 with IntelliSense™ combines fiber-optic speed with automatic in vivo calibration. The result is faster time to therapy, faster signal acquisition, and faster adaptation to rate and rhythm changes.
FORUMSView All (13)
0RepliesFri Dec 27 2024 | Falla en la carga de la batería Buenos tardes me podrían apoyar con una duda mi equipo no presenta ningún codigo de error sin embargo, no carga la batería alguien sabe cuanto tiempo lo tengo que dejar para que agarre carga la batería y se dejó desconectado por 15 dias Good afternoon, could you help me with a question? My device does not have any error code, however, the battery does not charge. Does anyone know how long I have to leave it for the battery to charge and it was left disconnected for 15 days? Reply |
3RepliesWed Apr 06 2022 | Electrical Test Fails Code #117 Can anyone help to solve the Electrical Test Fails Code #117 problem on our CS300? Thank you in advance Reply |
0RepliesMon Oct 11 2021 | All preprogramed Function Test in service mode will not initiate Unit has no error codes and passes POST. The device will enter service mode and I can select the different function tests, however, the preprogram function tests will not run after pressing open menu button. The other self tests work such as keypad test, display test. I can manually toggle each solenoid, but none of the programmed function test will initiate and run. I press the open menu button and it clicks, however the device seems to be waiting for the a start command and not getting it. Reply |
DOCUMENTS / MANUALSView All
FEATURES
[list] [*] CS300 has true one-button start-up [*] Automatically calibrates the fiber-optic pressure sensor in the patient and recalibrates every 2 hours or sooner should patient or environmental conditions change [*] Automatically evaluates and selects the best lead and trigger source [*] Automatically sets optimal timing [*] Automatically adjusts to changes in patient conditions without clinician intervention [/list]
FDA AlertsView All
Update On Device Failure Associated with Getinge's...
November 19, 2019 - Letter to Health Care Providers
Datascope/Getinge Recalls Cardiosave Hybrid, Cardiosave Rescue,...
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Class 1 Recall: Maquet Datascope Corporation, Intra-Aortic...
The firm received 106 reports of device malfunctions. There were zero injuries and one death.