What is the lead time for production?

The lead time is one month during peak season and 1-3 months during off-season.

Is the sterilization process safe against secondary pollution?

Yes, the sterilizing medium runs in a closed circulating system to prevent secondary pollution.

What certifications does the equipment hold?

The equipment holds CE, FDA, and ISO13485 certifications.

IV Solution Soft Bag Sterilization Machine

Name: Superior Liquid Sanitization System /Superlative Auto-Clave Supreme Sterilizer/IV Solution Soft Bag Sterilization Machine
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 1941655771

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$120,000.00-200,000.00

1 Piece

Product profile

Theory

Autoclave

Type

Pressure Steam Sterilization Equipments

Certification

CE, FDA, ISO13485

Model NO.

Customized IVEN -1

Electric Tension

380V

LCD Display

With LCD Display

Ultra High Temperature Alarm

Sterilization Information Recording and Printing

Material

Stainless Steel

Design Pressure

0.245 MPa

Design Temperature

139 Centigrade

Working Pressure

0-0.22MPa

Working Temperature

60-134 Centigrade

Power Supply

AC380V 50Hz

Compressed Air

0.6-0.8MPa

Transport Package

Wooden Package

Specification

3.2 x2 x1.5M

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

Dual Industry Application: Suitable for pharmaceutical liquid sterilization and food industry sealed package sterilization.

Closed Circulating System: Sterilizing medium runs in a closed system to prevent secondary pollution during operation.

High Heat Efficiency: Features good temperature uniformity with a wide temperature range for versatile use.

Anti-Pressure Protection: Equipped with anti-pressure protection device for safe operation on various containers.

LCD Display & Recording: Includes LCD display with sterilization information recording and printing capabilities.

Comprehensive Certification: Certified by CE, FDA, and ISO13485 for pharmaceutical and medical device compliance.

Flexible Customization: Offers full, minor, and flexible customization options based on samples or designs.

Stainless Steel Construction: Built with durable stainless steel material for longevity and hygiene.

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: ≤2.86h 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.