EDI for Reverse Osmosis System

Name: EDI for Reverse Osmosis System
Brand: Shandong Eagle Pharma Machinery Co., Ltd.
SKU: 2121469852

Shandong, ChinaShandong Eagle Pharma Machinery Co., Ltd.

US$8,000.00

1 Piece

Product profile

Customization

Available

Certification

ISO9001, RoHS, CE

Salt Rejection Rate

98.0%

Model NO.

ZG-D-003-HW

Application

Industry

Capacity

400 Gallon

Flow Rate

0.5,1.0,2.0,5.0,10.0

Product Resistivity

≥15.0

Ion Rejection Rate

≥99%

Wetted Material

SUS316L

Operating Temp

5 - 45

Documentation

Dq/Iq/Oq/Pq

Transport Package

Wooden Packaging

Specification

other

Trademark

WEMAC

Origin

China

HS Code

8421219990

Production Capacity

One Piece / Month

Key features

Continuous Deionization: Resin continuously regenerated via electric field, eliminating batch downtime.

Modular Scalable Design: Compact skid-mounted system allows flexible capacity expansion by adding modules.

FDA 21 CFR Part 11 Compliance: PLC control supports data acquisition and audit trails for regulatory compliance.

Eco-Friendly Operation: Chemical-free process eliminates hazardous waste from resin regeneration.

Deep Trace Removal: Highly efficient at removing CO2, Boron, and Silica weak electrolytes.

Validation Support: Provides FAT/SAT services and full DQ/IQ/OQ documentation packages.

Customizable Capacity: Standard capacity 0.5-50 m3/h, with customizable flow rates from 0.5 to 10.0.

Company profile

In-stock CapacityQuality AssuranceR&D CapabilitiesFull 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: ≤2.74h

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:Is the system customizable for different capacities?

Yes, the standard capacity ranges from 0.5 m3/h to 50 m3/h, but it is fully customizable. Flow rates can be adjusted from 0.5 to 10.0, and modules can be added to scale up capacity.

Q:Does the system comply with FDA regulations?

Yes, the intelligent PLC control system supports data acquisition and audit trails, ensuring compliance with stringent regulations like FDA 21 CFR Part 11.

Q:What validation documentation is provided?

We provide comprehensive validation support including Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), and a full documentation package including DQ, IQ, and OQ.

Q:How does this EDI system differ from traditional ion exchange?

Unlike traditional ion exchange which requires batch operation and chemical regeneration, our EDI system offers continuous deionization with no downtime and no hazardous chemical waste.

Q:What is the after-sales support structure?

We offer comprehensive after-sales support including remote fault diagnosis and on-site maintenance services to ensure minimal downtime and peak performance.