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High-Tech Bottle Sterilization Via Autoclave Steam Process/ Precision Steam Sterilization System for Industrial Bottle Containers
US$100,000.00-200,000.00
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

Ultra High Temperature Alarm

Sterilization Information Recording and Printing

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

Multi-Industry Application: Suitable for pharmaceutical LVP bottles and food industry sealed packages, drinks, and cans.
Anti-Pollution Design: Closing circulating system for sterilizing medium prevents second pollution during operation.
Comprehensive Certification: Certified by CE, FDA, and ISO13485 for industrial and pharmaceutical standards.
Smart Monitoring: Equipped with LCD display, ultra-high temperature alarm, and sterilization info recording.
Durable Material: Constructed from high-quality stainless steel for longevity and hygiene.
Flexible Customization: Offers full, minor, and flexible customization from samples or designs.
Turnkey Project Support: Manufacturer provides complete IV solution plant projects from design to training.

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: ≤1.46h 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 industries can this sterilizer be used for?
A:
It is widely applied in the pharmaceutical industry for liquid in glass, ampoule, and plastic bottles, and in the food industry for sealed packages, drinks, and cans.
Q:Does the system prevent contamination during sterilization?
A:
Yes, the sterilizing medium runs in a closing circulating system, which effectively prevents second pollution during the operating process.
Q:What certifications does the equipment hold?
A:
The equipment holds CE, FDA, and ISO13485 certifications.
Q:Is customization available for this machine?
A:
Yes, we offer full customization, minor customization, flexible customization, and customization from samples or designs.
Q:What is the minimum order quantity (MOQ)?
A:
The minimum order quantity is 1 Set.

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