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Pharmaceutical Water Distribution System for CIP
US$30,000.00
1 Piece

Product profile

Customization

Available

Application

Biotechnology Industry, Chemical industry, Food & Beverage Factory, Food Safety, Forensic Science, Pharmaceutical Industry

Capacity

Distribution

Model NO.

DN40

Certification

CE, FDA, GMP, ISO

Control System

Fully Automatic

Treatment Process

UV Disinfection

Warranty of core components

One Year

Design Standard

GMP

Number of Use Points

Number of Use Points

Flow Rate

Customized According to Project

Valve Type

Sanitary Diaphragm Valves

Power Supply

According to Local Standard

Instrumentation

Flow, Pressure, Temperature (Optional)

Sanitization Method

Hot Water / Chemical (Optional)

Operating Temperature

up to 90°C (Customizable)

Transport Package

Wooden

Specification

other

Trademark

WEMAC

Origin

China

HS Code

8419409090

Production Capacity

One Piece / Month

Key features

GMP Compliant Design: System designed according to GMP standards for biotechnology applications.
Continuous PW Supply: Provides continuous purified water replenishment for acid, alkali, and hot-water tanks.
Safe Isolation System: Features sanitary diaphragm valves and check valves to prevent chemical backflow.
Customizable Flow Rate: Flow rate is customized according to specific project requirements.
SS316L Material: Product-contact parts are made of high-grade SS316L stainless steel.
Flexible Sanitization: Supports optional hot water or chemical sanitization methods.
Final Rinsing Capability: Uses purified water for final rinsing to remove residual cleaning agents.

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: ≤3.18h

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 is the design standard for this system?
A:
The system is designed according to GMP standards to ensure compliance with pharmaceutical industry requirements.
Q:What material is used for product-contact parts?
A:
Product-contact parts are made of SS316L stainless steel to ensure hygiene and durability.
Q:Can the flow rate be customized?
A:
Yes, the flow rate is customized according to the specific project requirements.
Q:How is backflow protection achieved?
A:
Backflow protection is achieved through sanitary diaphragm valves, check valves, and hygienic isolation designs.
Q:What sanitization methods are supported?
A:
The system supports optional sanitization methods including hot water and chemical cleaning.

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