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High-End Good Quality Wfi Solution Preparation Purified Water Liquid Storage Mixing Tank
US$30,000.00-500,000.00
1 Piece
Product profile
Certification
ISO9001, CESalt Rejection Rate
99.5%Application
IndustryCapacity
100 GallonTransport Package
Wooden Case;Specification
customizedTrademark
IVENOrigin
ChinaProduction Capacity
CustomizedKey features
GMP Compliant Design: Conforms to GMP requirements with advanced technology and automatic control.
316L Stainless Steel: All materials touching liquid are made of high-quality 316L stainless steel.
Double Layer Structure: Upright double layer design with helical belt for steam heating or cooling water.
Customization Options: Supports full customization, minor customization, and flexible customization.
ISO9001 & CE Certified: Product holds ISO9001 and CE certifications for quality and safety.
Pharmaceutical Grade: Ideal for WFI solution preparation, purified water storage, and medical applications.
Company profile
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 is the material used for the tank?
A:
All materials that touch the liquid are made of 316L stainless steel.
Q:Does the tank meet GMP standards?
A:
Yes, the series tank conforms to GMP requirements with reasonable design and advanced technology.
Q:What is the capacity range available?
A:
The available capacities range from 1000L to 10000L across different models.
Q:Is customization available for this product?
A:
Yes, we offer full customization, minor customization, and flexible customization options.
Q:What certifications does the product have?
A:
The product is certified with ISO9001 and CE.
Send Inquiry
*To:
Shanghai Iven Pharmatech Engineering Co., Ltd.
Shanghai Iven Pharmatech Engineering Co., Ltd.*Content:
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