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Perfusor Compactplus Infusion Pump

Perfusor Compactplus Infusion Pump

B. Braun

Injection & Infusion
  • CE Marked medical device in the EU/EEA (class and exact designation per B. Braun Declaration of Conformity).
  • Designed and tested in accordance with IEC/EN 60601 1 (general safety), IEC/EN 60601 2 24 (particular infusion pump requirements) and related standards for medical electrical equipment.
  • Ingress protection rating IP34 against splashing fluids.
  • Meets B. Braun quality management system requirements for medical device manufacturing.
Syringe Infusion Pump

Description

The Perfusor Compactplus is a transportable electronic syringe infusion pump from B. Braun, designed to deliver precise, controlled infusion of medications and fluids. It features a high-resolution colour TFT display with wide viewing angle, guided syringe loading, an intuitive user interface with integrated DoseGuard drug library, semi-automatic drive and a long-life rechargeable lithium-ion battery. Built on the proven robustness of the original Perfusor compact range, the Compactplus is suitable for use across hospitals, ICUs, operating rooms, emergency care, ambulances and other clinical environments where reliable syringe-based infusion is required.

Bnefits

  • High-resolution colour display (approx. 2.4" TFT, 240 x 320 pixels, 262k colours) with wide 80° viewing angle for excellent visibility at the bedside.
  • Intuitive, self-explanatory user interface and guided loading to support quick, safe operation and reduce user error.
  • Integrated DoseGuard drug library with space for thousands of drugs and predefined parameters to support medication safety and standardised protocols.
  • Semi-automatic drive and assisted syringe loading for efficient, user-friendly handling.
  • Rechargeable lithium-ion battery providing extended operating time (around 10 hours at 5 ml/h) with short recharge time of approximately 3 hours.
  • Broad programmable basal rate range (typically 0.01–999.9 ml/h with 50/60 ml syringe) plus controlled bolus delivery capability.
  • High delivery accuracy (±2% in accordance with IEC/EN 60601-2-24) for precise infusion therapy.
  • Compatibility with a wide range of syringe brands and sizes (approx. 2/3, 5, 10, 20, 30, 50/60 ml) to fit local supply preferences.
  • Robust housing with IP34 protection against fluid ingress and an integrated pole clamp and handle for flexible mounting and transport.
  • Multiple power options (internal battery, AC mains via integrated power supply, DC from ambulance or docking station) for use in diverse clinical settings.

Indications

  • Continuous and intermittent intravenous infusion of medications and fluids using syringes in hospital and clinical settings.
  • Use in intensive care units, operating rooms, recovery rooms, emergency departments and step-down units where precise syringe-based infusion is required.
  • Infusion therapy for adults, paediatrics and neonates, as determined by institutional protocols and clinical judgement.
  • Transport applications (e.g. intra-hospital transfer, ambulance / emergency services) where a compact, battery-powered syringe pump is needed.
  • Use in general wards, oncology, cardiology and other departments requiring programmable syringe infusion therapy.

Composition

  • Electronic syringe infusion pump with integrated microprocessor control and semi-automatic drive mechanism.
  • Colour active-matrix 2.4" TFT display (approx. 240 x 320 pixels, 262k colours) integrated in the front panel.
  • Rechargeable lithium-ion battery module providing several hours of operation depending on flow rate.
  • Integrated power supply for connection to standard mains power via IEC power connector.
  • Mechanical syringe holding system with drive head, syringe claw mechanism, syringe holder and pole clamp on the rear side.
  • Housing constructed from durable medical-grade materials with ingress protection level IP34 against splashing fluids.
  • Interfaces including accessory connector, IR window/data interface and connectors for docking station or external power sources (depending on configuration).

Formulation

  • Syringe infusion pump designed for use with compatible disposable syringes from B. Braun (Perfusor, Omnifix) and other major manufacturers (e.g. BD, Terumo) in sizes from approximately 2/3 ml up to 50/60 ml.
  • Basal rate range typically 0.01–999.9 ml/h (with 50/60 ml syringe), programmable in fine increments in accordance with pump configuration.
  • Bolus rate capabilities in the approximate range of 1–1,800 ml/h, subject to syringe size and configuration.
  • Delivery accuracy around ±2% according to IEC/EN 60601-2-24.
  • Part of the B. Braun compactplus system, compatible with compactplus docking stations and data modules for multi-pump installations and data connectivity.

Packaging

  • Single Perfusor Compactplus syringe infusion pump unit.
  • Integrated pole clamp and carrying handle on the device.
  • Mains power cord compatible with the specified region (e.g. UK/EU plug).
  • User manual / instructions for use and, where applicable, quick-start or safety guides.
  • Device serial number and regulatory/identification labels on pump housing.
  • Additional accessories such as mounting hardware or docking station supplied separately depending on configuration or distributor offer.

Usage

  • Before use, read and follow the official Instructions for Use and all institutional protocols; only trained healthcare professionals should operate the device.
  • Check the pump housing, pole clamp, power connections and battery status for any damage or faults before connecting the device to a patient.
  • Select a compatible sterile disposable syringe (size and manufacturer approved for use with the Perfusor Compactplus) and fill it with the prescribed medication using aseptic technique; remove air and secure the plunger.
  • Mount the syringe in the pump’s syringe holder and engage the syringe claws/drive head following the guided loading instructions on the display.
  • Select or confirm the drug from the integrated DoseGuard drug library if used, or manually enter infusion parameters (rate, volume, duration) as per the prescription.
  • Connect the syringe line to the patient’s vascular access using appropriate IV lines and safety devices; ensure all clamps are correctly positioned and the line is primed, avoiding air in the tubing.
  • Start the infusion as directed; monitor the patient, infusion line and pump status regularly, paying attention to alarms, occlusion warnings, battery status and infusion progress.
  • For transport or battery operation, verify sufficient battery charge for the planned duration; connect to mains power or docking station when available to maintain charge.
  • At the end of infusion, stop the pump, clamp and disconnect lines according to institutional policy; dispose of used syringes and consumables as clinical waste.
  • Perform routine cleaning and functional checks as recommended by B. Braun and institutional biomedical engineering teams; schedule regular technical servicing and safety testing.

Contraindications

  • Use is contraindicated where syringe infusion pumps are not appropriate for the prescribed therapy or patient condition, as determined by a clinician.
  • Do not use with non-approved syringe types or sizes, or if syringe recognition is incorrect.
  • Do not use on patients if the pump shows error messages, visible damage or failed functional checks.
  • Do not use in environments that exceed the specified operating conditions for temperature, humidity, electromagnetic interference or altitude.
  • Use with caution or alternative equipment in MRI environments unless specifically rated and configured for such use.

Adverse Effects

  • Potential for under-infusion or over-infusion if infusion parameters are incorrectly programmed, Syringe is misloaded, or if alarms and warnings are ignored.
  • Risk of extravasation, infiltration or phlebitis at the infusion site if standard IV therapy precautions are not followed.
  • If air detection and line priming guidelines are not followed, there is a risk of air embolism through any IV infusion device.
  • Mechanical or electronic failure, although unlikely in a properly maintained device, can lead to interruption or alteration of infusion and requires prompt clinical action.
  • Improper cleaning or maintenance may lead to malfunction, alarm issues or contamination of device surfaces.

Storage Conditions

  • Store and transport the pump in a clean, dry environment within the temperature and humidity ranges specified by the manufacturer (typically standard hospital environmental conditions).
  • Protect from direct sunlight, excessive dust, vibration and shock during storage and transport.
  • When not in use for extended periods, store with the device switched off and, where recommended, connect periodically to mains power to maintain battery health.
  • Do not expose the device to immersion in fluids or high-pressure water jets; IP34 rating protects only against splashing water from any direction.
  • Keep out of reach of unauthorised persons; ensure only trained staff have access for clinical use.

Duration

Treatment duration is programmable and depends on the prescribed infusion rate and total volume to be delivered. The pump can support infusions ranging from short bolus deliveries to prolonged continuous infusions over many hours or days, within the technical limits and institutional protocols.

Onset

Onset of clinical effect depends entirely on the medication being infused, the infusion rate and patient-specific factors; the Perfusor Compactplus provides immediate, controlled start of infusion once activated and correctly set.

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