In the global nutraceutical and pharmaceutical industries, hygiene is not a feature—it is the foundation. EIXPACK systems are rigorously engineered to exceed the strictest sanitary, safety, and operational regulations of the European and North American markets.
All product contact parts (augers, hoppers, nozzles) are CNC-machined from premium 316L stainless steel, offering superior corrosion resistance against highly acidic or alkaline supplement formulations.
Our mechanical housings feature sloped surfaces and seamless welding. There are no hidden crevices, exposed threads, or dead corners where fine powders or bacterial growth can accumulate.
All non-metal contact materials, including O-rings, vacuum cups, and liquid hoses, are manufactured from 100% FDA-compliant, food-safe silicone and Teflon.
Cross-contamination between supplement batches is a critical risk for contract manufacturers. EIXPACK machinery features quick-release hoppers, augers, and dosing mechanisms. Operators can completely dismantle, wash down, and sterilize the entire product path in minutes—without using a single tool. This ensures 100% compliance while drastically reducing changeover downtime.
Every EIXPACK machine is built on a pharmaceutical-grade architecture designed to eliminate contamination risks and pass the most rigorous facility audits.
Transparent, high-impact acrylic shielding completely encloses moving parts. The machine instantly stops if a guard door is opened.
Control cabinets are powered by globally certified electrical components (Siemens, Schneider, Omron) to guarantee stable 24/7 voltage handling and fire safety.
Touchscreens and emergency stop buttons are strategically positioned to minimize operator fatigue and ensure instant access during critical moments.
Yes. We provide full traceability. Upon request, we supply documented Material Test Reports (MTRs) for our 316L stainless steel, as well as FDA compliance certificates for all silicone and polymer contact parts, ensuring your validation process goes smoothly.
Absolutely. Our equipment is actively running in strictly audited cGMP facilities across the United States and the European Union. The zero-dead-angle architecture and tool-less cleaning protocols are specifically engineered to satisfy FDA and EMA inspectors.
Tell us your technical requirements. Our engineering team will provide a tailored layout and ROI analysis.
Skip the back-and-forth. Send us your material specs and speed requirements for a custom machine layout.
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