Description
Precision Blending for Aseptic and Sterile Manufacturing
The V-10 V-Shape Mixer represents the forefront of mixing technology for critical pharmaceutical applications. Its unique V-shaped vessel creates a gentle yet highly efficient tumbling and folding action, ensuring a homogeneous blend without damaging delicate product structures. The integrated lifting platform and fully enclosed design are specifically designed to maintain sterility and operator safety, making it a cornerstone of any modern, compliant production line.
Key Technical Specifications & Operational Advantages
-
Sterile-Grade GMP Design: Constructed from high-quality AISI 316L stainless steel with a high-purity, electropolished finish (e.g., Ra ≤ 0.5 µm) on all product contact surfaces. The design features minimal dead legs and is fully drainable to support validated CIP/SIP processes.
-
Integrated Lifting Platform: The ergonomic lifting mechanism allows for safe and effortless raising and lowering of the mixing vessel, facilitating easy connection to charging systems and discharge points while minimizing operator strain and contamination risk.
-
Fully Enclosed «Shtany» System: The mixer is designed as a fully sealed unit to prevent dust generation and protect the product from external contaminants. This is critical for potent compound handling and maintaining an aseptic environment .
-
Efficient and Gentle Mixing: The V-shaped geometry ensures a three-dimensional mixing motion, achieving a blend homogeneity of over 99% without creating heat or shear forces that could degrade sensitive materials.
-
Advanced Control System: Operated via a user-friendly PLC interface with recipe management, data logging for full traceability, and interlocked safety guards on the lifting platform for operator protection.
Built for Compliance and Global Market Excellence
The V-10 mixer’s design and documentation package are tailored to help you meet and exceed international regulatory standards, including GMP, FDA 21 CFR Part 211, and EMA guidelines. This compliance is crucial for exporting your pharmaceutical products to markets in Southeast Asia, Africa, the Middle East, and Latin America.
| echnical Parameter | V-10 |
|---|---|
| Total Volume / Capacity (e.g., in liters) | Check the product’s technical datasheet or design specifications. |
| Working Capacity (typically 50-70% of total volume) | This is a key performance metric from engineering specs. |
| Motor Power (kW) and Rotation Speed (RPM) | Check the motor nameplate or product manual. |
| Lifting Platform Load Capacity & Travel (kg and mm) | Check the lifting mechanism specifications. |
| Material of Construction & Surface Finish (e.g., AISI 316L, Ra 0.4 µm) | Check the material certificates and polishing specifications. |
📜 Schedule virtual airflow visualization test.
💡 Mention your: Target market (EU/US/Global South), Active ingredient, Required throughput.
🔬 Schedule virtual factory acceptance test with our engineers.
🏷️ Request Compliance Audit: Free gap analysis with throughput simulation.
🔍Ready to Eliminate Production Bottlenecks?
💎Need Industrial Production Automation?
✅ GMP Compliance Guarantee
✅ 24/7 Multilingual Support
✅ 24-month performance guarantee
✅ Local technicians in 18 countries
📈Start small, get a free production layout designed for your growth trajectory. Scale smarter with engineering support!
📥Free line configuration for your products, throughput validation testing!
🎓Contact Specialists for Packaging Equipment:
📄 On-Demand Engineering: Product-specific configurations in 1-2 weeks.
🔧 Spare Parts Kits: Region-specific inventory for <24hr delivery.
🧼Compliance Roadmap:
- CE, EAC, ISO 9001 certifications.
- GMP-ready: 316L SS contact parts, CIP/SIP capabilities.
- ATEX options for chemical solvents.
