Advanced Multi-Effect Distillation System for Pure Water Solutions

Name: Advanced Multi-Effect Distillation System for Pure Water Solutions
Brand: Shandong Eagle Pharma Machinery Co., Ltd.
SKU: 2152653892

Shandong, ChinaShandong Eagle Pharma Machinery Co., Ltd.

US$5,000.00

1 Piece

Product profile

Customization

Available

Application

Biotechnology Industry, Chemical industry, Pharmaceutical Industry

Capacity

500 L/hr

Model NO.

Mixing system

Certification

CE, FDA, GMP, ISO

Control System

Fully Automatic

Treatment Process

Electrodeionization, Filtration, Ultrafiltration, UV Disinfection, Automatic Welding

Warranty of core components

One Year

Structure

Double Layers

Material

Connection with Liquid Using SS316L

Heat Preservation

Aluminum Silicate Needle Blanket

Transimiter

Temperature Transimiter

Transport Package

Wood Packing

Specification

500L/H

Trademark

WEMAC

Origin

Weifang

HS Code

8419409090

Production Capacity

500L/H

Key features

The whole system realizes closed loop online cleaning and online sterilization, avoids manual disassembly operation, reduces human introduced contamination risks.

CIP/SIP running parameters, alarm records and execution reports are automatically stored, satisfying pharmaceutical GMP audit requirements.

Adopt adjustable time temperature pressure multi parameter control strategy, optimize spray ball layout and fluid flow field, improve cleaning coverage and sterilization uniformity.

Company profile

High Repeat Buyers ChoiceMulti-language PioneerQuality AssuranceFull Customization

Shandong Eagle Pharma Machinery Co., Ltd.

Shandong, China

Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤1.63h

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:Can the CIP/SIP procedure adapt to multi-product switching production? Will it satisfy audit traceability requirements?

Yes. CIP/SIP sequences support recipe-based modular configuration for different products. All process parameters, alarms and execution reports will be automatically logged. Complete data records can be exported for review to fulfill GMP audit traceability demands. Based on your requirments to add the audit trial.

Q:What is the difference between this optimized CIP/SIP and traditional fixed-time cleaning mode?

Apart from time setting, the system monitors real-time indicators including conductivity, TOC and temperature to auto-judge cleaning endpoint, instead of simply following fixed duration. Combined with optimized flow-field and spray ball layout, it guarantees consistent cleaning effect while shortening cycle time and lowering water-steam consumption.

Q:Does the optimized CIP/SIP process need to stop the whole system for manual disassembly cleaning?

No. The system adopts fully closed-loop integrated CIP/SIP design. All inner wetted parts complete cleaning and sterilization in-situ without manual disassembly. It effectively eliminates cross-contamination risk caused by human intervention and meets GMP requirements for aseptic production.