KS-240 automates the preparation of patient-specific parenteral nutrition. The system enhances patient safety, traceability, workflow speed, quality assurance, flexibility, compliance and return on investment, while preventing ordering errors, compounding errors, manual additions, touch-contamination, drug loss, needle-based injuries and UV light effects.
Automated preparation removes manual additions and touch-contamination from the workflow.
Each preparation is recorded through the device workflow.
Gravimetric control verifies every addition by weight.
Dispensing runs at up to 1400 mL/min across 24 configured ports.
Configured ingredient access
Order entry and calculation
Manifolds, filters and tubing
NutriSoft provides TPN order entry and calculation, and is the point at which hospital system integration is assessed.
Electromechanical unit with 24-port valve actuators, peristaltic pump mechanism and control system. Includes built-in air bubble and congestion sensors for filling safety.
Embedded industrial-grade PC with touchscreen, running the KS-240 Device Operating Software.
Gravimetric control unit with integrated load-cell that self-calibrates with the calibration weight, and calculates the error ratio of each final product.
Certified 2 kg weight used for self-calibration of the scale unit.
Attaches all source containers: bags, bottles, syringes and vials.
| Weight | 34.5 kg (fully assembled) |
|---|---|
| Dimensions (w x d x h) | 76.7 x 52.5 x 46.0 cm |
| Minimum dispensing volume | 0.2 mL, in 0.01 mL increments |
| Maximum dispensing speed | 1400 mL/min (23.33 mL/sec) |
| Compound accuracy | ±10% at 0.2 mL, ±5% at 0.4 mL, ±2% at 1 mL, ±1% above 2 mL |
| Total number of ports | 24 |
| Operating temperature | 15 to 30 °C |
| Storage temperature | -34 to 65 °C |
| Power supply | AC 100-240 V, 50/60 Hz, 120 W, single phase |
| Noise level | Below 60 dB |
2014/35/EU low voltage and 2014/30/EU electromagnetic compatibility, in accordance with TS EN 60601-1, TS EN 61010-1 and TS EN 61326-1.
The answers below cover what hospital pharmacy, IT and technical teams ask most often. If your question is not here, our team will answer it directly.
Yes. KAPSAM systems exchange order and preparation data with HIS/EHR environments through HL7 and API integration, scoped per project with your IT team.
KAPSAM manufactures the sterile disposables used in the fluid path, including EVA bags, IV lines, filters and administration sets, assembled and sterilised in ISO 14644 compliant cleanrooms.
Installation and commissioning, on-site or virtual user training, preventive maintenance and technical support are provided by the KAPSAM service team or a trained distributor partner.
KAPSAM operates ISO 13485:2016, ISO 9001:2015 and ISO 14001:2015 certified systems and is audited by a notified body (CE 0425). Certificates can be downloaded from the Quality page.
Tell us about your application area, preparation volume and hospital systems. We will respond with the relevant technical and project information.