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Auto-Clave Water Treatment for Pharmaceutical & Medical Industry
US$30,000.00-500,000.00
1 Piece

Product profile

Application

Biotechnology Industry, Chemical Industry, Pharmaceutical Industry, Water Treatment Industry, Industry

Cleaning Method

Automated Cleaning

Filtration Capacity

1 L/hr

Model NO.

Customized IVEN -1

Material

Nylon, Polypropylene

Certification

ISO9001, CE

Salt Rejection Rate

99.5%

Capacity

100 Gallon

Transport Package

Wooden Case;

Specification

customized

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

Anti-Pollution Design: Closing circulating system prevents second pollution during the operating process.
Versatile Application: Suitable for pharmaceutical bottles, ampoules, plastic bags, and food industry sealed packages.
Safety Protection: Equipped with anti-pressure protection device for safe high-and-low temperature operations.
Flexible Customization: Supports customization from samples, designs, full customization, and minor adjustments.
Certified Quality: Product holds CE certification and manufacturer has ISO9001 certification.
100% Inspection: Finished products undergo 100% visual and function inspection before delivery.
Established Manufacturer: Factory established in 2005 with 19 years of export experience and 57 employees.

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: ≤2.21h 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:Can the machine be customized?
A:
Yes, we offer full customization, minor customization, and flexible customization from samples or designs.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 1 Set.
Q:What payment terms are accepted?
A:
We accept LC, T/T, D/P, PayPal, Western Union, and Small-amount payment.
Q:What is the lead time for production?
A:
The lead time is one month during peak season and 1-3 months during off-season.
Q:Is the sterilization process safe against pollution?
A:
Yes, the sterilizing medium runs in a closing circulating system which prevents second pollution.

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