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a Fully Automated Pharmaceutical Purified Water Generation, Storage, and Circulation Loop System 60000L+RO1
US$130,000.00-300,000.00
1 Set
Product specifications
Capacity
Product profile
Certification
ISO9001, CE, FDA, CE, FDA, GMP, ISOSalt Rejection Rate
99.5%Application
Industry, Biotechnology Industry, Chemical Industry, Food & Beverage Factory, Pharmaceutical IndustryModel NO.
250L/H-100000L/HCapacity
400 GallonControl System
Fully AutomaticTreatment Process
Chlorination, Electrodeionization, Filtration, Ozonation, Reverse Osmosis, Softening, Ultrafiltration, UV DisinfectionCapacity
60000L/HWarranty of Core Components
1 YearMaterial
SS316LMachinery Test Report
ProvidedElectrical Equipment
Siemens(Germany)Size
CustomizedProcessing Type
Reverse OsmosisTransport Package
Wooden CaseSpecification
60000L/HTrademark
WEMACOrigin
ChinaHS Code
8421219990Production Capacity
50000pieces/YearCompany profile
Shandong Eagle Water Treatment Technology Co.,LtdShandong, China
Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤1.45h
AI-Powered supplier vetting
SummaryThe supplier is identified as a trading company with biomass energy-related technical services in its stated business scope. It reports OEM and ODM capabilities, sample- and design-based customization, four production lines, and 50 quality-control staff. Export-related evidence is mixed: one slice states 41%–50% of sales come from exports and exports through agents and self-operated import/export rights, while another identifies the primary market as domestic and a separate slice states no overseas service locations or overseas agents. Service-management documentation is weak, with no written procedures or records for supplier assessment, corrective actions, or complaint handling. No SDK, no new products in the past year, and only two years of R&D engineer experience are reported. Financial and sustainability evidence is insufficient for a firm assessment, while customer-case evidence indicates validation-document experience and exports to more than 40 countries and regions.
After-Sales capabilityAfter-sales and service-management controls appear weak: there are no written procedures or records for service-capability assessment, corrective and preventive actions, or complaint handling. The supplier also reports no overseas warehouse, showroom, agent, branch, or offline trade-show capability, although it lists acceptable service terms and 13 qualified suppliers; these do not establish effective after-sales support.
R&D capabilityThe supplier reports ODM service and customization from samples and designs, but no available SDK, no new products during the past year, and only two years of total R&D-engineer experience. These explicit limitations outweigh the stated ODM capability for an overall innovation assessment.
Production capacityThe supplier reports four production lines, 50 quality-control staff, and combined facilities including flatting, cutting, and automatic welding machines. However, finished-product inspection has instructions but no written records, so production resources are demonstrated while process-documentation control is incomplete.
Customization capabilityBoth slices explicitly report customization from samples and from designs, and the supplier also states that it provides ODM services. This directly supports a demonstrated ability to handle customized products.
Client casesThe supplier states that its sales volume ranks first in China, that it has exported to more than 40 countries and regions, and that it has provided pharmaceutical validation documents including DQ, IQ, OQ, PQ, FAT, and SAT. These statements provide explicit evidence of broad market reach and sector-relevant customer experience, although no individual customer names are given.
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