- #Datascope cs300 operation guide install#
- #Datascope cs300 operation guide manual#
- #Datascope cs300 operation guide full#
- #Datascope cs300 operation guide software#
This sophisticated algorithm automatically selects the best lead and trigger source, sets optimal inflation and deflation timing, and still allows the clinician the ability to fine tune deflation timing.
#Datascope cs300 operation guide software#
The CS300 with INTELLISENSE'" software is designed to emulate an experienced user, allowing you more time to focus on your patient.
Fast QRS Recognition Enhanced R-Wave deflation performance STANDBY key: separate control from START key. Helium and Battery Level Icons Help Screen Availability Indicator. Timing control indicators display inflate and deflate settings. Unassisted Systolic and Diastolic Pressures Posted in 1:2 or 1:3 assist frequency. Automatic Scaling of AP and ECG waveforms. 
Color-coded trigger source indicator corresponds to signal waveform."Laptop style" display and keypad can be detached for remote opration Easier selection of available help menu screens.Intuitive arrow key trigger selection controls Fewer keys for simple operation.Built-in Service Diagnostics Software:Display/keypad convert to diagnostic program.
#Datascope cs300 operation guide manual#
Operation Mode Indicator:Auto, Semi Auto, Manual Intuitive IAB Status mIndicator. Fast Inflation Speeds Fast Deflation Speeds. #Datascope cs300 operation guide full#
Bright Full Color Display:High contrast screen with wide viewing angle and easy rotation/tilt Ergonomic Handle. 
Customers are instructed to complete and return the Medical Device Field Correction Response Form enclosed in the notice via fax to 1-97, or email at: If you are a distributor who has shipped any affected products to customers, please forward the Urgent Product Recall Medical Device Field Correction Notice to their attention for appropriate action. Until the affected unit is serviced for the potential fluid ingression into the IABP, users should review the operating instructions regarding cautions on placement of fluids and hanging of bags of fluid over the IABP. In the event the IABP fails to successfully cycle and clear the alarm, please remove the IABP from service and contact your local Maquet/Getinge Sales & Service Office. Maquet/Getinge recommends that users review the water condensation procedure to reduce the potential for condensation accumulation. Until the affected unit is serviced for the potential false blood detection alarm, clinicians should follow the instructions on the Blood Detection Alarm Help Screen to validate or clear the alarms. #Datascope cs300 operation guide install#
Be aware that customers with affected IABP unit(s) will be contacted by a representative of the Maquet/Getinge Service Team to schedule on-site service to install gaskets in the IABP unit(s) and upgrade software. Pursuant to the User Instruction Warnings, health care providers are instructed not to leave a patient unattended during IABP therapy. EMS agency owned, their need has diminished and. Check inventory to identify any affected IABP units that may be stored or are currently in use. Used DATASCOPE CS300 Balloon Pump For Sale - DOTmed Listing 2095090: This unit is in very good condition. The notice asked customers to please adhere to the following instructions: The firm recommends that the risks and benefits of using an affected CS100i, CS100, or CS300 IABP be assessed by the medical team for each patient when no alternative IABP or alternative therapy is available. RECOMMENDATIONS: On July 17, 2017, Datascope Corp./MAQUET sent affected customers an "Urgent Product Recall Medical Device Field Correction" notice informing them of the device's risks, and listing actions that should be taken to minimize the risk of patient harm until affected IABP units can be serviced. Lot Numbers: All Lots Manufactured Jto June 16, 2017īACKGROUND: Datascope Corp./MAQUET's CS100i, CS100, and CS300 Intra-Aortic Balloon Pumps are cardiac assist devices used to assist patients undergoing cardiac and non-cardiac surgery, and to treat patients with acute coronary syndrome or complications from heart failure. If a patient requires circulatory support with an IABP and the device does not work, or if therapy is stopped during use without a replacement IABP available, device failure may result in immediate and serious adverse health consequences, including death. ISSUE: Datascope Corp./MAQUET is recalling its CS100i, CS100, and CS300 Intra-Aortic Balloon Pumps manufactured Jto Jdue to False Blood Detection Alarm and Ingress of Fluid into the Intra-Aortic Balloon Pump. Models CS100i, CSO100, CS300 AUDIENCE: Risk Manager, Cardiology, Surgery
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