| Features and Benefits |
- Refurbished in an ISO 13485 Certified FDA registered Facility in an ISO 13485 Certified FDA registered Facility
- Technology that’s designed to calculate a patient pressure at an individual level and apply a minimum amount of tourniquet pressure needed to occlude a limb at a specific time for a specific patient
- Lower tourniquet cuff pressure reduces postoperative wound complications after TKA
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- Refurbished in an ISO 13485 Certified FDA registered Facility in an ISO 13485 Certified FDA registered Facility
- 105 to 130 VAC, 50/60 Hz electrical requirements
- 485 mA RMS max., 300 mA RMS Nominal line current
- 58 W max, 36 W Nominal Input power
- 50 to 475 mmHg Cuff pressure range
- ± 5 mmHg (50 to 475 mmHg) Pressure accuracy
- 0 to 240 Minutes; 1 minute increments Time alarm set ranges
- Rechargeable, sealed lead acid, 12 VDC, 2.3 AH battery
- 24 Hours maximum battery recharge time
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