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Syringe Pump

Single Channel Injection Pump HF-610E

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Single Channel Injection Pump HF-610E
Product data

Technical specifications

Key specifications and configuration details for Single Channel Injection Pump HF-610E

Model
HF-610E (single-channel)
Infusion Modes
Five modes: constant rate, time/total volume, drug dose by body weight, micro and programmable
Syringe Size
5~60ml, automatic recognition
Flow Rate Range
0.10~1500 ml/h
Flow Rate Increment
0.01 ml/h
Time Setting
1 second ~ 99 hours 59 minutes 59 seconds
Parameter Adjustment During Infusion
Total volume and flow rate can be modified during infusion
Rapid Purge
Supported, for rapid removal of air from the line
KVO Function
Adjustable from 0.10~5.00 ml/h to keep the vein open (KVO)
Occlusion Pressure
Dedicated pressure sensor, 20~150 kPa, sensitivity adjustable in 8 levels, with dynamic pressure display
Automatic Pressure Release
Automatic pressure release function
Display
Large display with 8-level adjustable brightness
Input Method
Physical numeric keypad (0~9) input
Syringe Management
More than 20 syringe brands built in; additional brands can be added, and after calibration all syringe brands are supported
Safety Design
Dual CPU design for safer infusion
Accuracy
Infusion error ≤ ±2%
Battery
2600mAh lithium battery, over 11 hours of continuous use for the single channel
Electrical Safety Classification
Class I equipment, CF-type applied part, IPX4 ingress protection (IP) rating
History Records
Stores up to 10000 history records
Intended Use
For intravenous drug infusion
Weight
2.1 kg
Dimensions
275mm × 145mm × 160mm
FAQ

Frequently asked questions about Single Channel Injection Pump HF-610E

Answers to common questions about product selection, use, and support.

How do I choose between the HF-610E and the HF-620A?
The HF-610E is a single-channel model weighing 2.1kg with a compact size, suitable for micro-infusion of a single drug and for transport. The HF-620A is a dual-channel model that can infuse two drugs simultaneously from one device, suitable for departments with frequent combined medication. The two have the same infusion modes, flow rate range and infusion error, so selection can be based on the department's medication protocol and space conditions.
What scenarios do the five infusion modes suit?
Constant rate mode: routine administration at a constant rate; time/total volume mode: the rate is calculated automatically from the set time and total volume; drug dose by body weight mode: the dose is calculated according to body weight; micro mode: low-speed, low-dose maintenance; programmable mode: stepped variable-rate infusion according to a preset program. The neonatal mode is particularly suitable for the neonatology department.
What is neonatal mode and why is it particularly suitable for the neonatology department?
Neonatal mode is designed for the characteristics of neonates, namely low body weight, very low drug doses and the significant effect of line volume. It delivers stable infusion at low speed and low dose, reducing dosing deviation caused by flow rate fluctuation, and is therefore particularly suitable for micro-dosing in the neonatology department.
What is the flow rate range and how precise is the adjustment?
The flow rate range is 0.10~1500 ml/h with a flow rate increment of 0.01 ml/h, allowing fine adjustment according to clinical needs. The time setting range is 1 second ~ 99 hours 59 minutes 59 seconds, and the total volume and flow rate can be modified during infusion.
What does an infusion error of ≤±2% mean?
It means the deviation between the actual infused volume and the set volume does not exceed ±2%; for example, when 100ml is set, the error is kept within 2ml. The device controls the flow rate at a constant speed by mechanical drive, and together with a flow rate increment of 0.01 ml/h it meets the requirements of precise micro-dosing in clinical practice.
How long does the battery last? Will infusion be interrupted during a power failure or transport?
The built-in 2600mAh lithium battery provides over 11 hours of continuous use for the single channel. The device has an automatic pressure release function and a handle on the body for intra-hospital transport; infusion can continue during a sudden power failure, reducing the risk of interrupted administration.
What is the 8-level adjustable occlusion sensitivity for? What is automatic pressure release?
Occlusion detection uses a dedicated pressure sensor with a range of 20~150 kPa and 8-level adjustable sensitivity, and the pressure value is displayed dynamically; an appropriate level can be set according to the drug, the line and departmental practice. The automatic pressure release function releases pressure automatically when line pressure is too high, reducing the effect of sustained high pressure on the line and the patient.
Which syringe brands are supported? Are dedicated consumables required?
It supports automatic recognition of 5~60ml syringes, has parameters for more than 20 syringe brands built in, and allows additional brands to be added; after calibration all syringe brands are supported. No dedicated consumables are required, so hospitals can continue to use their existing qualified syringes, reducing the cost of use.
What does the IPX4 ingress protection rating mean? How should it be cleaned and disinfected daily?
IPX4 means the device is protected against splashing water from any direction. For daily cleaning, wipe the housing with a damp cloth moistened with a neutral detergent, and avoid direct spraying or strongly acidic or alkaline disinfectants; take care to prevent liquid from entering the control panel and the gaps around the keys. Before cleaning, switch off the power and remove the syringe.
How are product certification and after-sales service guaranteed?
The Hepho Single-Channel Syringe Pump HF-610E is a Class II Medical Device with Medical Device Registration Certificate No. 粤械注准20192141164, supplied directly from the manufacturer by Olsmed Medical. Registration certificates and qualification documents required for hospital tenders and procurement can be obtained from Olsmed Medical, which also provides full lifecycle service including installation training, repair and maintenance, and spare parts supply.

Compliance Notice

This product is a medical device certified under NMPA, CE, ISO13485. It shall only be used by professional medical personnel in accordance with user manual and local regulations. Not for self‑diagnosis or self‑treatment. All information is for product display only, not medical advice.

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