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High-Tech Steam Sterilization for Industrial Bottle Containers/Precision Autoclave Steam Treatment for Bottle Sterilization
US$100,000.00-200,000.00
1 Piece
Product profile
Theory
AutoclaveType
Pressure Steam Sterilization EquipmentsCertification
CE, FDA, ISO13485Model NO.
Customized IVEN -1Electric Tension
380VLCD Display
With LCD DisplayUltra High Temperature Alarm
Ultra High Temperature AlarmSterilization Information Recording and Printing
Sterilization Information Recording and PrintingMaterial
Stainless SteelDesign Pressure
0.245 MPaDesign Temperature
139 CentigradeWorking Pressure
0-0.22MPaWorking Temperature
60-134 CentigradePower Supply
AC380V 50HzCompressed Air
0.6-0.8MPaTransport Package
Wooden PackageSpecification
3.2 x2 x1.5MTrademark
IVENOrigin
ChinaProduction Capacity
CustomizedKey features
CE, FDA, ISO13485 Certified: Meets international safety and quality standards for pharmaceutical and medical use.
Stainless Steel Construction: Durable material ensures hygiene and long-term reliability in industrial environments.
LCD Display & Recording: Features LCD screen with sterilization information recording and printing capabilities.
Anti-Pressure Protection: Built-in safety device prevents accidents during high-and-low temperature operations.
Multi-Industry Application: Suitable for pharmaceutical, food, and beverage industries including bottles and cans.
Flexible Customization: Offers full, minor, and design-based customization options to meet specific needs.
100% Finished Product Inspection: Every unit undergoes visual and functional inspection before delivery.
19 Years Export Experience: Manufacturer with nearly two decades of international trade and supply chain expertise.
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: ≤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 certifications does the sterilizer have?
A:
The equipment is certified with CE, FDA, and ISO13485 standards.
Q:Can the machine be customized?
A:
Yes, we offer full customization, minor customization, and options based on samples or designs.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 1 set.
Q:What are the working temperature and pressure ranges?
A:
Working temperature is 60-134 Centigrade and working pressure is 0-0.22MPa.
Q:How long is the lead time for production?
A:
Lead time is one month to three months, regardless of peak or off-peak seasons.
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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