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Destination System Water for Injection Steriling in Food /Pharma/Cosmatic Industrial
US$46,000.00
1 Piece

Product profile

Customization

Available

Application

Pharmaceutical Industry

Disposable

No

Model NO.

1000L/H

Injection Site

Intramuscular

Material

Glass, Plastic

Needle Gauge

21G

Safety Feature

Needle Guard

Usage

Diabetes Care, Medical, Pain Management, Vaccine Administration

Warranty

One Year

Feed Water

Purified Water

Heating Source

Industrial Steam

Separation Device

Three Stage Separation Device

Structure Form

Double Tube Plate Design

Insulation

Glass Fiber Needle Wire Mat

Control System

Full Automatic

Transport Package

Wood Packing

Specification

100L-3000L

Trademark

WEMAC

Origin

Weifang

HS Code

8419409090

Production Capacity

1000L/H

Key features

Multi-Effect Energy Saving: Industrial steam consumption ratio 1:0.21, no external cooling water required.
Pharmacopoeia Compliance: Meets CP2020, USP43, and EP10 standards for Water for Injection.
SS316L Material Construction: All parts contacting water/steam use SS316L with electro-chemical polishing.
Anti-Contamination Design: Double tube sheet design and argon protected welding prevent cross contamination.
Advanced Separation Tech: Three-stage separation: falling film, gravity, and spiral turbulence.
Full Automatic Control: HMI + PLC system with SCADA online monitoring and multi-level permissions.
High Quality Verification: Provides endoscopy photos, solder drawings, and passivation reports.
Customization Support: ODM and OEM services available for tailored industrial solutions.

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: ≤3.38h

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 this WFI generator 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:Does this system require external cooling water?
A:
No, the six-effect distilled water machine does not require external cooling water, as it utilizes secondary steam step-by-step in each effect.
Q:What is the industrial steam consumption ratio?
A:
The industrial steam consumption ratio is 1:0.21, and the raw water consumption ratio is 1:1.08, ensuring significant energy saving.
Q:What material is used for parts in contact with water?
A:
SS316L stainless steel is used for all parts in contact with raw water, water for injection, and secondary pure steam, with electro-chemical polishing for surface finish.
Q:How is cross-contamination prevented in the design?
A:
The system uses a double tube sheet plate design for the preheater, condenser, and evaporator, along with external welding processes to avoid cross-contamination.

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