Datascope - CS300
by Datascope

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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 (12)
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3

Replies
-Mark2022
2 years ago
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

0

Replies
-Denova Medical
3 years ago
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

1

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-normreeves
3 years ago
Maintenance required code #7
What does  Maintenance required code #7 mean?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.

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