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Wfi for Equipment Cleaning and Formulation Preparation
US$55,000.00
1 Piece

Product profile

Customization

Available

Application

Food Safety, Pharmaceutical Industry

Disposable

No

Model NO.

WFI 3000L/H

Injection Site

Intramuscular

Material

Stainless Steel

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

3000L

Trademark

WEMAC

Origin

Weifang

HS Code

8419409090

Production Capacity

3000L/H

Key features

Pharmacopoeia Compliance: Meets CP2020, USP43, and EP10 standards for Water for Injection.
Energy Efficient Design: Industrial steam ratio 1:0.21 and water ratio 1:1.08 without external cooling.
Anti-Contamination Structure: Double tube sheet plate design with internal expansion and external welding.
High Purity Material: All wetted parts constructed from SS316L stainless steel.
Advanced Separation System: Three-stage separation using falling film, gravity, and spiral turbulence.
Full Automatic Control: HMI + PLC system with SCADA for online monitoring and data acquisition.
Superior Surface Finish: Electro-chemical polishing ensures high surface quality and weld integrity.
Comprehensive Verification: Includes endoscopy photos, welding drawings, and passivation reports.

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: ≤2.55h

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 the WFI meet?
A:
The produced water meets the specifications of Chinese Pharmacopoeia (CP2020), United States Pharmacopoeia (USP43), and European Pharmacopoeia (EP10).
Q:Does the system require external cooling water?
A:
No, the six-effect distilled water machine does not require external cooling water.
Q:What is the material 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.
Q:How is the control system configured?
A:
It adopts HMI + PLC full-automatic control with SCADA for online monitoring, data acquisition, and at least three levels of permission.
Q:What is the warranty period for this equipment?
A:
The equipment comes with a one-year warranty.

Send Inquiry

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