Decide the flow behaviour before the device:
| Parameter | Typical specification | Note |
|---|---|---|
| Flow rate range | Adjustable, typically 1–20 ml/h class | Confirm against your lowest and highest therapy rate |
| Reservoir volume | 100 / 200 ml class | Sets duration at the selected rate |
| Delivery mode | Continuous, optional bolus | Bolus where patient-triggered dosing is used |
| Rate setting | Selectable at set-up | Changeable for the patient, unlike elastomeric |
| Power | Battery, disposable or rechargeable per design | Confirm expected runtime against therapy duration |
| Fluid path | Disposable set | Connector matched to the access device |
Note: specifications vary by configuration. Confirm rate range, runtime and connector against the therapy before ordering.
An electronic device introduces questions a mechanical one does not have:
Three situations justify the electronic device: the rate changes between patients or over the treatment course; the delivered volume has to be recorded for the patient's notes; or the required rate falls outside what fixed-rate mechanical devices offer. If your protocols use one rate per therapy and there is no documentation requirement, an elastomeric pump does the same job with fewer failure modes and a lower cost per case.
Configurations typically span the low single-digit to roughly 20 ml/h, which covers post-operative analgesia, regional block infusion and general ward use. Confirm the range against your lowest and highest therapy rate rather than the nominal figure — paediatric dosing and higher-rate adult infusions can sit at opposite ends of the specification.
Configurations intended for documented therapy can report delivered volume, which is one of the strongest reasons to choose an electronic device over a mechanical one — the infusion becomes a recordable observation rather than an assumption. Confirm the specific recording and data-export behaviour for the configuration you are evaluating.
Runtime is specified against therapy duration, and the device behaviour on power depletion is documented — including any alarm. This is a question worth asking explicitly of any electronic infusion device: how it fails matters more than how it performs when everything is nominal. Confirm the runtime margin covers your longest protocol.
Occlusion is detected by pressure and signalled by alarm, with the detection threshold and response documented in the device specification. Because an occluded line that is not detected simply stops delivering therapy without the patient or staff knowing, occlusion detection is treated as a patient-safety function and documented rather than described loosely.
Yes. A powered device adds electrical-safety, electromagnetic-compatibility and software documentation to the technical file, and this affects the registration dossier for your market. We provide the manufacturer-side documents; tell us the destination country and we will confirm the additional items your registration holder will need.
Parent and related categories:
Anesthesia Consumables ·
Disposable Portable Infusion Pump ·
Nursing Consumables
OEM & manufacturing:
OEM Infusion Consumables ·
OEM & ODM Services ·
Factory Audit & Visit
Regulatory guides for your market:
EU MDR Import Requirements ·
Saudi Arabia SFDA Registration ·
All Regulatory Guides
Who we supply:
Hospital Procurement ·
Pain Management Clinics
Technical reading:
Electronic Infusion Pump Applications ·
Closed IV Infusion Standards ·
Sterile Syringes and Needles
Deciding between an electronic and a mechanical infusion pump?
Tell us how often rates change in your protocols and whether you record delivered volumes. We will tell you which device is the better buy for your caseload — including if the simpler one is the right answer.
We will recommend the configuration that fits, including where a mechanical pump is the better choice.