Lonrecon Hospital Infusion Pump for ICU, General Ward and Clinical Medication Delivery | LR-IP8081N

The Lonrecon LR-IP8081N hospital infusion pump is designed for ICU, general ward, emergency, and project-based clinical deployment. It supports controlled medication delivery, operational stability, staff standardization, and scalable institutional use, with customization and project delivery support available.

Model: LR-IP8081N
Device Type: Hospital Infusion Pump
Pumping Mechanism: Curvilinear peristaltic
IV Set Compatibility: Compatible with standard IV sets
Flow Rate Range: 0.1–2000 mL/h
Infusion Modes: Rate Mode, Time Mode, Body Weight Mode, Dose Mode, Sequence Mode, Ramp Up/Down Mode, Micro-Infusion Mode, Drop Mode
Flow Rate Accuracy: ±5%
VTBI Range: 0.10 mL–99999.99 mL
Bolus Rate: 50–2000 mL/h
Bolus Volume: 0.1–50 mL
Air-in-Line Detection: Ultrasonic detector
Air Bubble Level: 40–800 uL, adjustable
Occlusion Sensitivity: 20–130 kPa, adjustable
KVO Function: Automatic KVO with on/off function
Core Operational Functions: Dynamic pressure monitoring, key lock, standby, historical memory, drug library
Alarm System: Occlusion, air-in-line, door open, near end, end program, low battery, end battery, motor malfunction, system malfunction, drop error, standby alarm
Connectivity / Expansion: Docking station compatible, automatic multi-channel relay, optional wireless
Power Supply: AC 100–240V, 50/60Hz
Battery: 14.4V rechargeable lithium battery, 2200mAh
Battery Life: Up to 10 hours at 25 mL/h
Operating Environment: 5°C–40°C; 15%–80% RH
Ingress / Safety Classification: Class II, Type CF, IPX3
Dimensions: 240 × 87 × 176 mm
Weight: <2.5 kg

Hospital Infusion Pump for Reliable Clinical Deployment

Why This Hospital Infusion Pump Matters in Clinical Environments

The LR-IP8081N is designed as a hospital-running IV infusion pump for controlled medication and fluid delivery across ICU, general ward, recovery, and emergency workflows. For procurement teams, a smart infusion pump matters not because it adds a longer feature list, but because it helps standardize infusion practice across departments, supports safer parameter setting, and reduces dependency on manual adjustment alone.

Why Hospitals Choose This Type of Device

Hospitals choose this type of IV infusion pump when they need one platform to support multiple delivery requirements in daily care. The LR-IP8081N supports rate mode, time mode, body weight mode, dose mode, sequence mode, ramp up/down mode, micro-infusion mode, and drop mode. In project deployments, a smart infusion pump with drug library support, adjustable occlusion sensitivity, and air-in-line detection is easier to align with department protocols than a basic single-mode device. The device also supports standard IV sets and a wide flow-rate range, which helps simplify equipment planning across varied clinical scenarios.

Operational Stability and Continuity in Hospital Use

From an operational perspective, this IV infusion pump supports flow-rate adjustment without stopping therapy, automatic KVO logic, historical memory, alarm management, battery-backed transport continuity, and optional wireless connectivity. These characteristics make the smart infusion pump more suitable for hospitals that need continuity between bedside care, intra-hospital transfer, and centralized equipment management. Compatibility with docking station use and automatic multi-channel relay also supports more structured deployment in higher-acuity or higher-workload departments.

Impact on Training, Maintenance and Daily Operation

For hospital administrators and biomedical teams, the value of LR-IP8081N is not only in infusion delivery, but in easier standardization. A unified mode structure, alarm framework, key lock function, self-checking logic, and stored historical memory can help reduce training inconsistency between shifts and departments. In maintenance terms, a rechargeable battery, clear alarm architecture, and deployment-ready interface logic can support more predictable lifecycle management in institutional use. For project-based supply, this model is better positioned as an operational device for clinical systems rather than a standalone retail product. FDA guidance also emphasizes that safe pump use depends not only on the device itself, but on training, access to instructions, and proper risk management processes.

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