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Factory Direct Multi-Standard Purified Water Tank
US$30,000.00-500,000.00
1 Piece

Product profile

Certification

ISO9001, CE

Salt Rejection Rate

99.5%

Application

Industry

Capacity

100 Gallon

Transport Package

Wooden Case;

Specification

customized

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

316L Stainless Steel Construction: All liquid-contact materials use 316L stainless steel for superior corrosion resistance and hygiene.
GMP Compliant Design: Conforms to GMP requirements with advanced technology and automatic control systems.
Double Layer Insulation: Upright double-layer structure with helical belt for steam cooling or hot water heating and heat preservation.
High Salt Rejection Rate: Features a 99.5% salt rejection rate ensuring high-purity water output for pharmaceutical applications.
Polished Welding Finish: Internal polishing and polished welding parts ensure a smooth, clean surface that prevents bacterial growth.
Versatile Capacity Options: Available in volumes ranging from 1000L to 10000L to suit various industrial production scales.
Factory Direct Supply: Directly supplied from the manufacturer with 19 years of export experience and ISO9001 certification.

Company profile

Shanghai Iven Pharmatech Engineering Co., Ltd.
Years of Export ExperienceLow MOQPatents AwardedProduct Certification
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: ≤2.00h 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.

Product Q&A

Q:What materials are used for the water tank?
A:
All materials that touch the liquid are made of 316L stainless steel. The outside warming board uses mirror or ground board, and welding parts are polished.
Q:What is the salt rejection rate of this system?
A:
The system has a salt rejection rate of 99.5%, ensuring high-quality purified water.
Q:Is the tank suitable for pharmaceutical applications?
A:
Yes, the tank conforms to GMP requirements and is designed for use in pharmaceuticals, medicals, and biochemical industries.
Q:What are the available volume capacities?
A:
The available volumes range from 1000L to 10000L, including models LCG-1000 through LCG-10000.
Q:How does the temperature control work?
A:
The double-layer structure includes a helical belt in the interlayer that can pass steam for heating or cooling water for cooling, with heat preservation material filled inside.

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