V-Type Pharmaceutical Dry Powder Mixers Shipped to Thailand GMP Pharmacy Factory

Client Cooperation Background

1. Open mixing generates massive powder dust, causing raw material cross-contamination and failing annual FDA & Thai FDA hygiene inspection
2. Uneven manual blending leads to unstable active ingredient content, high batch rejection rate
3. Heavy manual material feeding increases labor cost and raw material waste during transfer
   After comparing multiple domestic pharmaceutical equipment manufacturers, the client selected our VH series V-type tumbling mixers for full 316L sanitary contact parts, zero dead-angle internal structure, PLC automatic timing control and complete CE certification meeting Southeast Asian pharmaceutical import standards.

Core Pharmaceutical-Grade Equipment Advantages

1. Mirror Polished 316L Stainless Steel Mixing Barrel
   All material contact sections adopt medical-grade 316L stainless steel with Ra≤0.8μm mirror polishing, seamless welding without cleaning dead corners. The barrel cover uses quick-open clamp structure, tool-free disassembly to support CIP online cleaning and high-temperature disinfection, fully matching GMP clean room requirements for tablet, capsule and granule production.
2. Uniform Gentle Tumbling Mixing Without Material Degradation
   Two inclined barrels rotate reciprocally, materials split and recombine continuously under gravity diffusion mixing. No high-shear stirring blades to damage heat-sensitive herbal extracts and probiotic powder; mixing uniformity reaches RSD≤3%, mixing cycle adjustable from 4–12 minutes according to raw material fluidity. Optional intensifier bar solves agglomeration of sticky herbal fine powder.
3. PLC Intelligent Safe Control System
   10-inch touch screen stores 20 groups of mixing parameter recipes, supports automatic timing rotation, speed adjustment and complete production data traceability. Equipped with safety interlock limit switch: machine stops rotating immediately once safety guardrail opens to eliminate operator injury risk, mandatory safety configuration for pharmaceutical clean workshops.
4. Low Residue & Low Maintenance Design
   Discharge outlet with quick-release butterfly valve, complete material discharge with less than 0.1% residual powder, greatly saving high-value pharmaceutical raw materials. Drive system adopts silent gear reducer, low vibration and low noise; wearing parts are universal standard specifications with long service cycle, reducing later maintenance downtime.

Wide Application in Southeast Asian Pharmaceutical Industry

Complete After-Sales Support for ASEAN Pharmaceutical Clients

• 12-month full warranty for core motor, reducer and PLC control components
• Full Thai & English bilingual operation, cleaning and validation manuals
• Overseas engineer on-site installation, commissioning and GMP equipment validation training after container arrival
• Fast sea freight spare parts channel with delivery cycle within 8 working days

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