New & Used Intra Aortic Balloon Pump, Kontron Medical

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Item Details

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Item Price (USD)

Year manufactured

763820056

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Device: Intra Aortic Balloon Pump
Manufacturer: Kontron Medical
Model: KAAT K2000

Location: United States, New York
Rating: 88%

1500 1,500

-

527697242

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Device: Intra Aortic Balloon Pump
Manufacturer: Kontron Medical
Model: KAAT K2000

Location: United States, New York
Rating: 88%

Negotiable

-

892989628

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Device: Intra Aortic Balloon Pump
Manufacturer: Kontron Medical
Model: KAAT 11 7200

Location: United States, Florida
Rating: 100%

2000 2,000

-

Intra Aortic Balloon Pump may also be referred to as :

Pump, Intra-Aortic Balloon | Pump, Balloon | Circulatory Assist Unit, Intra-Aortic Balloon | Intra-Aortic Balloon Pump Console | Heart Pump | Diastolic Augmentation Pump | Circulatory Assist Unit, Diastolic Augmentation | Balloon Pump | Intra-Aortic Balloon Pump

Tips for buying Intra Aortic Balloon Pump

1. To allow for timing adjustments, the intra-aortic balloon pump monitor should display inflation and deflation intervals on the pressure waveform.
2. Data to be displayed on the diastolic augmentation pump includes the following: ECG, heart rate, arterial pressure, and alarm conditions. Other optional data to be displayed may include: balloon pressure, volume, and setup instructions.
3. Automatic and manual timing adjustments should be offered by the intra-aortic balloon pump unit. ECG and pressure triggering modes should be available. The necessary controls and displays, as well as a chart recorder, should all be part of the pump console.
4. Moving the pumps should not present any physical challenges to the clinical staff. The intra-aortic balloon pump needs to protect against disconnection and catheter displacement during transport. It should be strong enough to handle mechanical shocks it may encounter during transport.
5. Audible and visual alarms should be part of the intra-aortic balloon pump, and they should alert users in the following conditions: trigger loss, vacuum/pressure loss, trigger change, balloon disconnect, balloon over inflate, balloon leak, power loss, inflation during asystole, and significant heart rate change.
6. Alarms should be clear and noticeable since the intra-aortic balloon pump is a life-support system. Audible and visual alarms for critical parameters should be activated and deflate the balloon. When the alarm is silenced, a visual display should clearly show the disabled alarm.
7. Before purchasing such a diastolic augmentation pump, facilities need to look at its ability to use and support this technology in an effective manner. Not every facility finds the intra-aortic balloon pump to be appropriate for its needs.