
KIRO Fill
KIRO Fill - Automated Compounding Device for Sterile Non-Hazardous Preparations
KIRO Fill
KIRO Fill is an automated compounding device focused on the production of non-hazardous sterile preparations. Automating critical and repetitive processes such as capping and filling ensures consistency and reduces the potential for human error. The system supports multiple final container types and allows for simultaneous loading, unloading, and compounding, optimizing workflow efficiency. Its compact design, comparable to a standard six-foot laminar flow hood, makes it a practical addition to various pharmacy settings. Like KIRO Oncology, KIRO Fill integrates seamlessly with hospital information systems to enhance operational efficiency.
Material Preparation and Identification Area
Touchscreen for user instructions and confirmations
Barcode/datamatrix and radio frequency identification (RFID) systems to identify and control source and final containers used
Loading/Unloading Area
Manual loading and unloading
Barcode scanning of raw materials
RFID for in process tracking
Up to 20 loading positions for final products:
– Syringes: 3mL, 5 mL, 10 mL, 20 mL, 30 mL and 50 mL
– Luer bags: 50 mL, 100 mL, 250 mL, 500 mLSource bags and vials of different brands and sizes supported
LED-guided positioning
Compounding Area
Two automated units working in parallel handle transfer syringes to withdraw solutions from source containers and fill syringes via luer lock connections
Automatic capping of syringes with tamper-evident, luer-lock or luer slip caps
Control of used source containers and drug left-overs
Gravimetric control over the source bag that weights the bag before and after every dose withdrawal
Air Treatment area
ISO 5 aseptic environment in material preparation, loading, and unloading areas and in lower compounding area
Horizontal air flow with HEPA H14 filters
Continuous monitoring of:
– Air flow operation
– Non-viable particle counts
– TemperatureOptional monitoring of non-viable particle counts
KIRO Fill Key Benefits
Safety
ISO 5 aseptic compounding environment protects sterility during production of non-hazardous compounded sterile preparations
Automation minimizes risk of contamination and increases dosing accuracy
Repetitive stress and needle-stick injuries are mitigated
Guided and software-controlled manual loading and unloading of supplies for enhance patient safety
Control and Traceability
Loading and automated compounding processes are controlled by means of barcode scanning and RFID identification
Batch reports and labels for the compounded preparations generated to ensure traceability through production
Flexibility and Efficiency
Unique design and small footprint facilitate high throughput and optimization of workload, workflow, and staff time while consuming minimal valuable cleanroom space
Integrates two automated units working in parallel
Accomodation of a large variety of sizes and types of source and final containers
Batch compounded sterile preparations
Optimized the use of medication and left-overs