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CE and ISO Certified Pharmaceutical Water Distiller Equipment
US$50,000.00-250,000.00
1 Piece
Product profile
Application
Pharmaceutical & MedicalCertification
CE, GMP, ISOTechnique
Membrane Separation TechnologyModel NO.
Customized IVENMaterial
Steinless SteelFunction
Water PurificationGrade
200 SeriesProcessing Service
WeldingSurface Finish
TshsPrecision
High PrecisionVoltage
380VComputerized
ComputerizedCustomized
CustomizedCondition
NewWarranty
1 YearAfter-Sales Service
Field Installation, Commissioning and TrainingTransport Package
Wooden PackageSpecification
Customized500-10000LTrademark
IVENOrigin
ChinaProduction Capacity
CustomizedKey features
High Purity WFI Production: Generates ultra-pure water compliant with Chinese Pharmacopoeia standards for injections and blood products.
Premium Material Construction: Constructed from 304 or 316L stainless steel ensuring durability and hygiene for pharmaceutical applications.
Multi-Effect Energy Efficiency: Multi-effect design reduces steam consumption and energy usage without requiring additional cooling water.
Flexible Operation Modes: Available in full-automation, semi-automation, and manual operation to suit diverse user requirements.
Comprehensive Certifications: Certified with CE, GMP, and ISO standards, ensuring safety and quality for global pharmaceutical markets.
Customization Options: Offers customization from samples, designs, and flexible minor adjustments to meet specific project needs.
Versatile Industry Application: Ideal for hospitals, pharmaceutical, medical, electronic, food, and drinking water industries.
One-Year Warranty Support: Includes 1-year warranty with field installation, commissioning, and training services provided.
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: ≤2.25h 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 certifications does the water distiller have?
A:
The equipment is certified with CE, GMP, and ISO standards to ensure compliance with international quality and safety regulations.
Q:What materials are used in construction?
A:
All components and parts are made of high-quality 304 or 316L stainless steel to ensure purity and durability.
Q:Is customization available for this equipment?
A:
Yes, we offer customization from samples, designs, full customization, and flexible minor customization options.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 1 set.
Q:What is the lead time for production?
A:
The average lead time is 1-3 months, depending on the season and specific order requirements.
Send Inquiry
*To:
Shanghai Iven Pharmatech Engineering Co., Ltd.
Shanghai Iven Pharmatech Engineering Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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