Medicine Bottle 500ml PE Extrusion Blow Molding Machine 80FDE-4S

Pharmaceutical packaging demands the highest standards of consistency, cleanliness, and traceability. The MEPER 80FDE-4S(100) extrusion blow molding machine is configured to meet the rigorous requirements of 500ml PE pharmaceutical and medicine bottle production. The machine's 4-cavity synchronous molding architecture, driven by a 75mm screw extruder achieving 85kg/h plasticizing rate, delivers bottle-to-bottle consistency that pharmaceutical fillers rely on for automated packaging line compatibility. With 15-zone precision die head thermal management (16.5kW) and 3-zone screw heating (15.3kW), the 80FDE-4S maintains the tight process control window essential for producing containers used in oral liquid medicines, syrup formulations, and health supplement packaging. The 120kN clamping system with 480x500mm mold accommodation supports production of bottles with child-resistant closure-compatible neck finishes and tamper-evident seal geometries required by pharmaceutical regulations.

• Validated Process Control Architecture: The 15-zone die head heating system with independent PID controllers provides the documented, repeatable thermal profiles essential for pharmaceutical packaging validation protocols and process qualification documentation.
• Batch Consistency Verification: 120kN clamping force applied through precision-ground platens with 540mm toggle stroke ensures cavity-to-cavity dimensional repeatability within pharmaceutical tolerance specifications for automated filling line compatibility.
• Cleanroom-Ready Design: The enclosed drive system with 22kW extruder motor and 15kW oil pump motor features sealed bearing assemblies and accessible surfaces for cleaning protocols, supporting installation in controlled environments adjacent to pharmaceutical filling suites.
• Material Traceability Support: The 75mm screw with 24:1 L/D processes pharmaceutical-grade PE formulations with complete plastication, supporting batch record documentation of processing parameters for regulatory compliance.
• Precision Neck Geometry: Maximum mouth mold diameter of 35mm accommodates pharmaceutical closure systems including child-resistant caps, tamper-evident bands, and graduated dosing cups for oral liquid containers.
• Documented Thermal Profile: 3-zone screw heating (15.3kW) with 0.14kW fan cooling provides logged temperature data across the extrusion process, supporting material processing validation requirements common in pharmaceutical packaging operations.
• Scalable Production Architecture: 4-cavity simultaneous output with 85kg/h plasticizing capacity provides pharmaceutical packaging operations with production scalability from pilot batches to full commercial manufacturing runs.

The 80FDE-4S(100) serves pharmaceutical and healthcare packaging operations with specialized capabilities for medical container production. Oral liquid medicine manufacturers utilize the machine for 500ml cough syrup and analgesic suspension bottles requiring consistent fill volumes and child-resistant closure compatibility. Health supplement and vitamin producers benefit from the machine's production of opaque PE bottles that protect light-sensitive formulations while maintaining precise dosing-cap compatibility. Clinical nutrition and enteral feeding product packagers leverage the 4-cavity output for cost-effective production of 500ml feeding solution containers with standardized neck finishes. Veterinary medicine manufacturers also use the system for producing animal health product bottles within the same size range. The machine's documented process control capabilities support pharmaceutical quality system requirements for container consistency verification, while the 0.4 m³/min cooling water and 1.5 m³/min compressed air consumption keep operational costs predictable for regulated manufacturing environments.

Each 80FDE-4S(100) undergoes extended factory acceptance testing including 72-hour continuous operation validation, statistical process capability analysis on critical bottle dimensions (CpK target: greater than or equal 1.33), material processing documentation for pharmaceutical-grade PE, and comprehensive hydraulic and pneumatic system integrity verification. Machines are prepared for export with ISPM-15 certified fumigated wooden pallets, pharmaceutical-industry-compatible packaging materials (non-shedding, cleanable), VCI anti-corrosion treatment on all exposed metal surfaces, and environmental data loggers available upon request for transit condition monitoring. Documentation package includes detailed installation qualification (IQ) and operational qualification (OQ) guideline documents, CE and ISO9001:2008 certificates, and complete English-language technical manual with PLC program backup. Standard 12-month warranty with priority technical support for pharmaceutical industry customers; extended warranty and on-site commissioning with validation support available.