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GMP Standard Double Stage RO Pharmaceutical Purified Water Generation System
US$49,999.00
1 Piece
Product profile
Customization
AvailableApplication
Biotechnology Industry, Chemical industry, Food & Beverage Factory, Pharmaceutical IndustryCapacity
500 L/hrModel NO.
PW-500Certification
CE, FDA, GMP, ISOControl System
Fully AutomaticTreatment Process
Chlorination, Electrodeionization, Filtration, Reverse Osmosis, Softening, UltrafiltrationWarranty of core components
1 YearControl
Full AutomaticSystem
PLC+HMIMaterial
Sanitary PipelineProcess
RO Membrane SystemTransport Package
Wooden PackageSpecification
Stainless steel 304 and 316LTrademark
WEMACOrigin
Weifang, ChinaHS Code
8421219090Production Capacity
300 Pieces/YearCompany profile
Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤3.32h
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.
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*To:
Shandong Eagle Pharma Machinery Co., Ltd.
Shandong Eagle Pharma Machinery Co., Ltd.*Content:
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