Audible and visual alarm for occlusion, empty, low battery, end of infusion, door open, wrong setting etc, which gain patents. HD LCD Display, high capacity words, friendly user interface, dynamically display working status.KVO: KVO (keep-vein-open) automatically opens as infusion is completed. Power Source: AC100-240V, 50/60Hz; Internal Battery. Language: English, Poland, Latvian, Russian etc. Infusion Rate 0.1ml/h---1200ml/h (1ml/h step, input 016 when set the rate from 800 to 1200ml/h). Rate Accuracy within±5% (after correct calibration).
Purge Rate 100ml/h---1200ml/h(can be calibrated). Volume Limit 0ml---9999ml Total Infusion Volume 0---9999.9 ml. Alarm Pressure High:800mmHg±200mmHg(106.7kPa±26.7kPa) Medium:500mmHg±100mmHg(66.7kPa±13.3kPa) Low:300mmHg±100mmHg(40.7kPa±13.3kPa).Alarms end of injection, occlusion, door open, bubbles in the tube, wrong setting. Low battery, AC power pulled out etc.
Internal rechargeable Li battery volume=1,600mAh 4 hours internal battery backup. Bubble Detector ultrasonic wave detector, detection sensitivity =25µL. KVO Speed 1ml/h---5ml/h (1ml/h step). Dimension 140mm (L)x 157mm (W)x 220mm (H).
Infusion set brand Compatible with any brand. Forbidden Not support blood Infusion. Package 1pc per each Carton, 2.8KG; 24cm (L) x 26cm (W) x 31cm (H).
Only unused, undamaged and original condition item can be qualified for a return. We're one of the largest online dental suppliers based on many qualified manufacturers in China. We supply all dental items with very nice qualities and the best reasonable prices for worldwide dentistry students, dentists and other professionals. Looking forward to our friendly & win-win cooperation.Statement:The sale of this item may be subject to regulation by the U. Food and Drug Administration and state and local regulatory agencies. The Fingertip Pulse Oximeter is certified with the US FDA 510K No.
K070371, the CE & TUV of Europe and it is on the Australian Register of Therapeutic Goods (ARTG) with the code 136606. The Powered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number:K132989. The Powered Surgical Instrument / Hair Remove Device is certified with the US FDA 510(k) Number:K180353. The Powered Surgical Instrument / Hair Remove System is certified with the US FDA 510(k) Number:K141973.Massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA 510(k) Number:K161892.