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Advanced Pharmaceutical Water Purification System for GMP Compliance
US$40,000.00
1 Piece

Product profile

Customization

Available

Certification

ISO9001

Salt Rejection Rate

1

Model NO.

3000L/H

Application

Industry

Capacity

2000L

Applicable Industries

Pharmaceuticals Laboratories Hospitals

Does It Support Inspection

Yes

Does It Support Customization

Yes

Electrical Control System Brand

Siemens

Transport Package

Wooden Case

Specification

304

Trademark

WEMAC

Origin

Weifang Shandong

Production Capacity

1/30days

Key features

GMP & 21 CFR Compliance: Supports electronic signatures and records for GAMP 5 and 21 CFR Part 11 audit tracking.
316L Stainless Steel: Main material is 316L stainless steel with electrochemical polished, gas-protected automatic welds.
Siemens Control System: Features HMI+PLC full-automatic control with Siemens electrical components and multi-level security.
Dual Softener Pre-treatment: Dual softeners operate in series with automatic regeneration via sophisticated valve group.
Modular & Compact Design: Compact structure with aesthetically pleasing layout for easy operation and maintenance.
Energy Saving Operation: Variable frequency control reduces energy consumption and microbial growth during standby.
Comprehensive Documentation: Provides endoscope photos, pressure test reports, and passivation reports for quality assurance.
Customizable Capacity: Output is customizable, with reference capacity of 3000L/H for industrial applications.

Company profile

Shandong Eagle Pharma Machinery Co., Ltd.
In-stock CapacityQuality AssuranceR&D CapabilitiesFull Customization
Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤3.01h

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 compliant with GMP and 21 CFR Part 11?
A:
Yes, the system supports optional electronic signature and record capabilities to facilitate audit tracking in alignment with GAMP 5 requirements and 21 CFR Part 11 compliance.
Q:What is the main material used for the pipes?
A:
The main material is 316L stainless steel. Pipes are stretch-bent to minimize welding, and welds are gas-protected automatic welding with electrochemical polishing.
Q:Does the system support customization?
A:
Yes, the output is customizable. The reference capacity is 3000L/H, and it can be tailored for pharmaceuticals, laboratories, and hospitals.
Q:What brand is the electrical control system?
A:
The electrical control system brand is Siemens, featuring HMI+PLC full-automatic control with an intuitive interface and configurable authority levels.
Q:How does the pre-treatment stage work?
A:
It uses dual softeners operating in series with the capability to regenerate alternately via a sophisticated valve group, delivering 100% water supply capacity.

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