Robotized palletizer K.Pak 820C

stand-alonefor the pharmaceutical industryend-of-line

Overview
The K.Pak 800 series performs precise case handling and consistent placement onto pallets for pharmaceutical packaging lines. Its configurable architecture adapts to specific palletizing patterns, case formats and line-integration requirements. Optional interfaces with line management and serialization systems support traceability and quality verification. The K.Pak 800 series is designed for integration with Körber conveying, packaging, inspection and software solutions to enable end-to-end packaging lines.

Your benefits

• Pharma-first design: hygienic layout tailored to pharmaceutical production and cleaning procedures.
• Smooth product handling: precise case transfer and placement to protect products and facilitate transport.
• Flexible line solution: usable as a standalone unit or integrated into a complete packaging line.
• Configurable: adaptable pallet patterns and options to fit various case formats and pallet sizes.
• Traceability ready: optional connection to line management and serialization systems for verified traceability.

Technical Details (table)
Case size (lxwxh mm) | Pallet size (lxw mm) | Output (cases/min)
Minimum | 200x140x100 | 1000x800 | 7
Maximum | 610x410x400 | 1220x1016 | 5

Features / Technical specifications

• Series: K.Pak 800 series
• Model: K.Pak 820C (example shown)
• Case size range: min 200 x 140 x 100 mm — max 610 x 410 x 400 mm
• Supported pallet sizes: min 1000 x 800 mm — max 1220 x 1016 mm
• Throughput: up to ~7 cases/min (small-case example) and ~5 cases/min (large-case example), depending on format and configuration
• Precise handling and accurate pallet placement
• Configurable palletizing patterns and machine options
• Optional integration with line management and serialization systems for traceability
• Compatibility with Körber conveying, packaging, inspection and software ecosystems for full-line integration
• Hygienic, pharmaceutical-oriented design to facilitate cleaning and support GMP considerations