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Advanced Pharmaceutical Distillation System with Comprehensive Audit Trail
US$28,000.00
1 Piece
Product specifications
500L/H
Product profile
Customization
AvailableApplication
Food Safety, Pharmaceutical Industry, CosmeticsDisposable
NoModel NO.
500L/HInjection Site
IntramuscularMaterial
Glass, PlasticNeedle Gauge
21GSafety Feature
Needle GuardUsage
Diabetes Care, Medical, Pain Management, Vaccine AdministrationWarranty
One YearFeed Water
Purified WaterHeating Source
Industrial SteamSeparation Device
Three Stage Separation DeviceStructure Form
Double Tube Plate DesignInsulation
Glass Fiber Needle Wire MatControl System
Full AutomaticFeed Water Consumption
≤550L/HIndustrial Steam Consumption
≤135kg/HCooling Water Consumption
≤190L/HTransport Package
Wood PackingSpecification
500L/HTrademark
WEMACOrigin
WeifangHS Code
8419409090Production Capacity
500L/HKey features
Multi-Effect Energy Saving: Industrial steam consumption ratio 1:0.21 and raw water 1:1.08 for significant energy efficiency.
Pharmacopoeia Compliance: Meets CP2020, USP43, and EP10 standards for Water for Injection (WFI) quality.
Advanced Separation Tech: Three-stage separation using falling film, gravity, and spiral turbulence for high purity.
Full Automatic Control: HMI + PLC system with SCADA online monitoring, data acquisition, and multi-level permissions.
Premium Material Quality: SS316L used for all parts contacting raw water, WFI, and steam to prevent contamination.
No External Cooling Needed: Design eliminates need for external cooling water for capacities over 1000 L/H.
Audit Trail System: Equipped with comprehensive audit trail and recorder for key data logging and compliance.
Certified Safety Standards: CE and ISO certified with electrochemical polishing to ensure surface finish and hygiene.
Company profile
Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤4.35h
AI-Powered supplier vetting
SummaryThe supplier is identified as a trading company with a broad technical, equipment, software, and engineering-related business scope. It demonstrates professional technical R&D positioning, 3D software design, ODM, OEM, and multiple customization options. Quality and service procedures are partly established, including inspection instructions, complaint handling, supplier assessment, and corrective-action records. However, the supplier has only one quality inspector, has exported for one year, lacks raw-material traceability labels and written quality records, and has no overseas warehouse or showroom. Innovation evidence is mixed because no new products were reported in the past year and no SDK is available. Financial information is present only as year references, without sufficient evidence to assess credibility.
Supplier typeThe supplier is explicitly classified as a Trading Company. Its stated scope covers technical services, technology development, equipment sales, software development, IoT services, industrial engineering design, and equipment repair, indicating a technically oriented trading and service business rather than a clearly documented manufacturer.
After-Sales capabilityThe supplier has documented and followed procedures for complaint handling, supplier service-capability assessment, and corrective/preventive actions, and it reports in-stock service capability. However, it lacks overseas warehouse and showroom capabilities, so the evidence supports structured service handling but not comprehensive overseas support.
R&D capabilityThe supplier reports professional technical R&D capability, 3D software design, ODM services, and OEM services for popular brands. Counterbalancing this, it reported no new products during the past year and has no available SDK, so the evidence supports design and development services but not strong recent product innovation.
Customization capabilityThe supplier explicitly provides customization from samples, full customization, and customization from customer designs. It also offers 3D software design and ODM services, providing clear evidence of broad customization capability.
Product Q&A
Q:What pharmacopoeia standards does the distilled water meet?
A:
The produced water for injection meets the specifications of Chinese Pharmacopoeia (CP2020), the United States Pharmacopoeia (USP43), and the European Pharmacopoeia (EP10).
Q:Is external cooling water required for operation?
A:
No external cooling water is required. The six-effect distilled water machine uses secondary steam step-by-step, and no cooling water is needed if the capacity is over 1000 L/H.
Q:What is the warranty period for this equipment?
A:
We provide a one-year warranty for the pharmaceutical distiller.
Q:What materials are used for parts contacting water and steam?
A:
SS316L stainless steel is used for all parts in contact with raw water, water for injection, and secondary pure steam to ensure safety and prevent contamination.
Q:Does the system support data monitoring and audit trails?
A:
Yes, it features a Full Automatic HMI + PLC control system with SCADA online monitoring, data acquisition, and an audit trail system to record key parameters like conductivity and temperature.
Send Inquiry
*To:
Shandong Eagle Pharma Machinery Co., Ltd.
Shandong Eagle Pharma Machinery Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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