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Autoclave Superior Water Purification Equipment/Sterilization Machine/Normal Saline Soft Bag Sterilization Machinery
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
Multi-Industry Application: Suitable for pharmaceutical liquid sterilization and food industry sealed packages.
Anti-Pollution Design: Closing circulating system prevents second pollution during operation.
Comprehensive Certifications: Equipped with CE, FDA, and ISO13485 certifications for safety.
Advanced Monitoring: Features LCD display, ultra-high temperature alarm, and recording printing.
Durable Material: Constructed with high-quality stainless steel for longevity.
Flexible Customization: Offers full, minor, and flexible customization from samples or designs.
Turnkey Project Support: Provides complete IV solution plant services from design to installation.
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 industries can this sterilizer be used for?
A:
It is widely applied in the pharmaceutical industry for liquid sterilization in various containers and in the food industry for sealed packages, drinks, and cans.
Q:What is the working temperature range?
A:
The working temperature range is 60-134 degrees Celsius, with a design temperature of 139 degrees Celsius.
Q:Does the machine prevent secondary pollution?
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 have?
A:
The equipment holds CE, FDA, and ISO13485 certifications.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 1 set.
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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