What is the lead time for production?

The lead time is one month during the off-season and 1-3 months during the peak season.

Is online disinfection supported?

Yes, the system can choose thermal disinfection for RO membranes and EDI, realizing online hot water disinfection.

What is the working water temperature range?

The working water temperature range is 5-35 degrees Celsius.

RO System Water Purifier Plant Project

Name: RO System Water Purifier Plant Project
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2045189465

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-200,000.00

1 Piece

Product profile

Certification

ISO9001, CE

Salt Rejection Rate

99.5%

Application

Industry

Capacity

100 Gallon

Max Working Pressure(MPa)

10000 MPa

Volume

1000L-10000L

Height

2000-3900mm

Diameter(mm)

900-2000

Diameter

900-2000mm

Transport Package

Wooden Case;

Specification

customized

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

High Salt Rejection: Achieves a 99.5% salt rejection rate for superior water purification quality.

Customizable Dimensions: Volume ranges from 1000L to 10000L, with height and diameter fully customizable.

Modular Design: Compact structure with modular design for easy installation and scalability.

Advanced Control System: Features PLC automatic control and optional paperless or paper recording modes.

Online Disinfection: Supports online hot water disinfection for RO membranes and EDI systems.

Energy Efficient: Pumps controlled by frequency to optimize energy consumption and stability.

Certified Quality: Manufactured under ISO9001 and CE certification standards for reliability.

Low Operating Cost: Designed for low investment and low operating costs in high salinity areas.

Company profile

Years of Export ExperienceLow MOQPatents AwardedProduct Certification

Shanghai Iven Pharmatech Engineering Co., Ltd.

Shanghai, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 19 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤2.16h CertifiedTerms of Payment: LC, T/T, D/P, etc.

AI-Powered supplier vetting

SummaryThe supplier is a combined company offering pharmaceutical and medical production equipment, including vial, ampoule, prefilled syringe, oral liquid, tablet, capsule, visual inspection, packaging, and logistics solutions. It provides extensive customization and integrated services such as process design, equipment selection, installation, commissioning, and validation. Export activity is substantial, with 71%–90% of sales from exports and 19 years of export experience. Quality assurance, ISO9001:2015 certification, CE capability, manufacturing contracts, and finished-product inspection instructions are documented strengths. However, the supplier lacks in-stock, overseas warehouse, overseas showroom, overseas agent or branch capabilities, and has no written procedures for service assessment, corrective actions, or complaint handling. R&D evidence is limited: no SDK, no new products in the past year, and no ODM or major-brand OEM services. No specific customer cases are provided.

CertificationsThe supplier reports an ISO9001:2015 certificate and CE certification capability, providing explicit evidence of quality-management and product-compliance credentials. However, the slices do not specify the scope, validity period, or products covered by these credentials.

After-Sales capabilityThe supplier lists installation, commissioning, validation, maintenance, debugging, repair, training, and integrated consulting services, and provides equipment installation-related offerings. Nevertheless, it has no overseas agents or branches, no overseas warehouse or showroom, and no written procedures or records for complaint handling, service assessment, or corrective and preventive actions, indicating an operational weakness in documented after-sales management.

R&D capabilityThe supplier has customization-oriented R&D services, but reports no available SDK, no new products during the past year, no ODM service, and no OEM service for popular brands. These explicit limitations indicate weak evidence of current product innovation and platform development.

Production capacityThe supplier covers multiple pharmaceutical equipment production lines, including vial and ampoule, prefilled syringe and cartridge, oral liquid, tablet and capsule, inspection, packaging, and logistics systems. It has valid manufacturing contracts with each affiliated subcontractor, follows finished-product inspection instructions uniformly, and reports quality assurance, although no quantitative production-capacity data is provided.

Customization capabilityThe supplier explicitly offers customization from samples, designs, full customization, minor customization, and flexible customization. Its integrated solution includes process design, conceptual and construction design, equipment selection, model customization, installation, commissioning, and validation, demonstrating broad customization coverage.