What certifications does the product have?

The product holds CE, GMP, and ISO certifications.

What is the minimum order quantity?

The minimum order quantity is 1 set.

What are the lead times for delivery?

Lead time is one month to three months, regardless of peak or off-peak seasons.

Pharmaceutical Water Purification Equipment & High-Purity Water Distillation System

Name: Pharmaceutical Water Purification Equipment & High-Purity Water Distillation System
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2070842445

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-250,000.00

1 Piece

Product profile

Application

Pharmaceutical & Medical

Certification

CE, GMP, ISO

Technique

Membrane Separation Technology

Model NO.

customized

Material

Steinless Steel

Function

Water Purification

Grade

200 Series

Processing Service

Welding

Surface Finish

Tshs

Precision

High Precision

Voltage

380V

Computerized

Customized

Condition

New

Warranty

1 Year

After-sales Service

Field Installation, Commissioning and Training

Transport Package

Wooden Package

Specification

Customized500-10000L

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

High-Purity WFI Production: Generates Water for Injection compliant with Chinese Pharmacopoeia (2010) without heat source contamination.

Premium Stainless Steel Construction: All components made of 304 or 316L stainless steel for durability and hygiene.

Multi-Effect Energy Efficiency: Models with six or more effects operate without requiring additional cooling water.

Flexible Operation Modes: Available in full-automation, semi-automation, and manual operation to suit different user needs.

Comprehensive Industry Coverage: Ideal for pharmaceutical, medical, electronic, food, and drinking water industries.

Full Customization Options: Offers full customization, minor customization, and flexible customization from samples or designs.

1-Year Warranty Coverage: Includes 1-year warranty with field installation, commissioning, and training services.

Multiple Certification Standards: Certified under CE, GMP, and ISO standards for quality assurance.

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: ≤1.80h 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.