UMH-V5 4.3-Inch Touch Screen Infusion Pump

UMH-V5 Touch Screen Infusion Pump

The UMH-V5 is a medical infusion pump designed for controlled intravenous fluid and medication
delivery in hospitals, intensive care units, emergency departments, operating rooms, general wards,
and patient-transfer environments.

A 4.3-inch color touch screen provides direct access to infusion parameters and operating information.
The pump supports multiple infusion modes, configurable IV-set calibration, real-time pressure monitoring,
adjustable safety parameters, and rechargeable battery operation for flexible clinical workflows.

Key Features

• 4.3-Inch Color Touch Screen:
  Allows direct parameter entry, adjustment, and monitoring through an intuitive touch interface.
• Flow Rate up to 2000 mL/h:
  Supports an adjustable flow range from 0.1 to 2000 mL/h with fine rate adjustment for different infusion requirements.
• Multiple Infusion Modes:
  Supports multiple programmed infusion workflows together with a Micro mode for low-rate applications.
• Editable IV-Set Library:
  Supports compatible standard IV sets and can store up to 200 editable IV-set brand configurations.
• Drug Error Reduction System:
  DERS configuration can support a drug library containing more than 2000 drug entries, depending on software configuration.
• Parameter Adjustment During Infusion:
  Selected infusion parameters can be adjusted without stopping an ongoing infusion, according to the configured operating mode.
• Dynamic Pressure Monitoring:
  Graphic and numeric pressure display helps operators monitor infusion-line pressure changes in real time.
• Adjustable Occlusion Settings:
  Provides five selectable pressure levels across approximately 50–900 mmHg.
• Adjustable Air-Bubble Detection:
  Air-in-line detection sensitivity can be configured according to the clinical setup and IV-set requirements.
• Anti-Bolus Function:
  Designed to reduce unintended bolus delivery after release of an occlusion condition.
• Dual Rechargeable Batteries:
  Uses two 2600 mAh lithium-polymer batteries and supports more than 10 hours of operation at 25 mL/h under specified test conditions.
• IP44 Enclosure:
  Designed with an IP44-rated enclosure for clinical use and patient-transfer environments.

Typical Applications

The UMH-V5 is suitable for controlled IV infusion where accurate flow adjustment, medication programming,
pressure monitoring, and safety alarms are required.

• Intensive care units
• Emergency departments
• Operating rooms
• General hospital wards
• Postoperative care
• Infusion and treatment rooms
• Patient transfer
• Ambulance and transport applications where the supplied configuration and documentation are appropriate

Infusion Modes and Parameter Control

The UMH-V5 supports multiple infusion modes for different treatment protocols. Available modes and drug-library
functions should be configured according to the intended clinical workflow and hospital requirements.

A dedicated Micro mode is available for low-rate infusion applications. The touch-screen interface allows
operators to review and modify selected parameters including rate, target volume, air-detection level, and
occlusion-pressure level.

Available functions may vary by software version and supplied configuration, so the required infusion modes
should be confirmed before ordering.

IV Set Compatibility and Calibration

The UMH-V5 is designed for use with compatible standard IV infusion sets. Because tubing dimensions,
elasticity, and flow characteristics vary between manufacturers, the selected IV set should be correctly
calibrated before clinical use.

The system can store up to 200 editable IV-set brand configurations, allowing hospitals and distributors
to configure frequently used infusion sets for routine operation.

Buyers should provide the intended IV-set brands and specifications before ordering so compatibility and
calibration requirements can be reviewed.

Drug Library and DERS Support

The UMH-V5 platform supports a Drug Error Reduction System with a configurable drug library containing
more than 2000 drug entries, depending on the installed software configuration.

DERS functionality can assist with programmed infusion workflows by providing predefined drug-related
parameters and limits. Drug-library content, dose limits, clinical protocols, and software configuration
should be validated by the purchasing medical institution before clinical deployment.

Pressure Monitoring and Safety Functions

The infusion pump provides dynamic pressure monitoring with graphic and numeric pressure information.
Five selectable occlusion-pressure levels cover approximately 50 mmHg to 900 mmHg.

Air-bubble detection sensitivity can also be adjusted according to the infusion setup. An anti-bolus
function is designed to reduce unintended fluid delivery when an occlusion is released.

Alarm types, alarm thresholds, pressure response, and air-bubble settings should be confirmed according
to the supplied software version and operating manual.

Technical Specifications

Battery and Patient-Transfer Operation

The UMH-V5 supports AC mains power, external 10–16 V DC input, and dual rechargeable lithium-polymer batteries.
This power configuration provides flexibility for bedside use, intra-hospital transport, and other situations
where continuous mains power may not be available.

With the specified dual 2600 mAh battery configuration, operating time is stated at more than 10 hours at
25 mL/h under defined test conditions. Actual runtime can vary with battery age, screen usage, flow rate,
alarm activity, operating temperature, and other conditions.

Before Ordering

Infusion-pump configuration, IV-set calibration, drug-library software, battery configuration, and regulatory
documentation may differ by destination market and supplied version. Please confirm the following before ordering:

• Required quantity
• Destination country
• Local voltage and plug type
• IV-set brands and tubing specifications
• Required flow-rate range
• Required infusion modes
• Need for Micro mode
• DERS and drug-library requirements
• Air-bubble detection requirements
• Required occlusion-pressure settings
• Battery-runtime requirements
• External DC power requirements
• Pole clamp and mounting requirements
• Ambulance or patient-transport application requirements
• Required regulatory and import documentation

If CE documentation, EN 1789-related documentation, or other market-specific certificates are required,
please specify the destination country and required documents so the current applicable documentation can
be confirmed before quotation.

Request a Quote for the UMH-V5 Infusion Pump

Send UMY Medical your required quantity, destination country, IV-set specification, infusion-mode requirements,
drug-library needs, battery requirements, and intended clinical application. Our team can confirm the available
configuration, accessories, documentation, lead time, and quotation.

Email:
[email protected]
WhatsApp / Tel:
+86 199 2588 4840

Contact UMY Medical

UMH-V5 Infusion Pump FAQ

What is the flow rate range of the UMH-V5?

The UMH-V5 supports a specified flow rate range of 0.1–2000 mL/h with a minimum adjustment increment
of 0.01 mL/h. Actual infusion performance depends on the selected IV set, calibration, and operating configuration.

Can the UMH-V5 use different IV-set brands?

Yes. The system is designed for compatible standard IV sets and can store up to 200 editable IV-set brand
configurations. The intended infusion set should be correctly calibrated before clinical use.

Does the UMH-V5 support a drug library and DERS?

The platform supports Drug Error Reduction System functionality with a configurable library containing more
than 2000 drug entries. Available DERS functions depend on the supplied software configuration and should be
validated according to the hospital’s medication protocols.

What should be confirmed before ordering the UMH-V5?

Buyers should confirm the required infusion modes, IV-set brands, DERS and drug-library functions,
air-bubble and occlusion settings, battery requirements, mounting accessories, destination country,
and required regulatory documentation before ordering.