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Vhp Pass Boxes for Safe Transfer of Diagnostic Device Components
US$15,000.00
1 Piece
Product profile
Customization
AvailableOptional Accessory
Drum, Timer Switch, Intercom, Sterilization Lamp, FloodlightNoise
40-60dbSurface Treatment
ElectroplatingInside Diameter
600*600*600mmInstallation
Embedded or FloorOperating Principle
Vaporized Hydrogen PeroxideType
Inflatable Sealing and Interlocking SystemName
Vhp Pass BoxMaterial
SUS304#Power
220V 50/60 HzColor
Stainless SteelApplication
Dusbiopharmaceuticals/ Medical Devices/Food IntryCertification
CE ISO GMPInterlock
Inflatable Sealing and Interlocking SystemTransport Package
StandardSpecification
customizedTrademark
PharmaOrigin
SuzhouHS Code
8414609090Production Capacity
20sets/WeekKey features
VHP Sterilization Technology: Utilizes Vaporized Hydrogen Peroxide to eliminate 99.9999% of microorganisms.
Double Door Interlock System: Ensures only one door opens at a time to prevent cross-contamination.
High-Quality Stainless Steel: Constructed from SUS304 or SUS316 for corrosion resistance and durability.
Adjustable Sterilization Time: Sterilization cycle ranges from 30 to 120 minutes based on requirements.
Touch Screen Control: Features LCD touch screen with multi-language support for easy operation.
Comprehensive Safety Protection: Equipped with overpressure protection, leakage detection, and automatic alarms.
Flexible Customization Options: Supports full customization, sample-based customization, and flexible options.
Company profile
CertifiedBusiness Type: Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Full Customization, etc. CertifiedExport Year: 9 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤2.06h
AI-Powered supplier vetting
SummaryThe supplier is identified as a manufacturing factory in Suzhou, China, supplying pharmaceutical machinery, packaging machinery, cleanroom equipment and materials, laboratory equipment, and related products. It provides 3D software design, ODM, OEM, SDK, and multiple customization options, indicating broad technical and customization capabilities. Production evidence includes a stated annual cleanroom capacity of 10,000 square meters and a 500 m² manufacturing plant, with most materials reportedly stocked and shipment possible within seven days except for specially made air conditioners. Quality assurance is stated, but documented service procedures, complaint-handling records, corrective actions, and approved-supplier lists are absent. No overseas warehouse, showroom, agents, branches, or offline trade-show participation are reported. No new products were developed in the past year. Customer project experience is described for national and international pharmaceutical and laboratory projects, but...
Supplier typeThe supplier is explicitly classified as a factory and operates in manufacturing and processing, with business scope covering pharmaceutical machinery, packaging machinery, cleanroom equipment, water treatment equipment, laboratory equipment, and related products. This supports classification as a specialized industrial equipment manufacturer rather than only a trading company.
After-Sales capabilityThe supplier has quality assurance, but reports no written procedures or records for service assessment, corrective and preventive actions, or effective customer-complaint handling. It also has no overseas warehouse, showroom, agents, or branches, limiting demonstrated overseas service infrastructure.
R&D capabilityThe supplier is identified as a professional technical supplier, provides 3D software design, ODM services, OEM services for well-known brands, and an available SDK. However, it also reports no new products during the past year, so current innovation output is mixed rather than consistently demonstrated.
Production capacityThe supplier states annual cleanroom productivity of 10,000 square meters, operates a 500 m² manufacturing plant, and reports fast production with most materials stocked and shipment within seven days except for specially made air conditioners. These statements provide explicit evidence of production capacity and responsiveness, although the capacity data covers cleanrooms rather than every product category.
Customization capabilityThe supplier offers customization from samples, full customization, and flexible customization, together with 3D software design, ODM, OEM, and customized tools and parts. Its broad cleanroom and pharmaceutical equipment scope further supports the ability to deliver tailored industrial solutions.
Product Q&A
Q:What sterilization technology does the VHP Pass Box use?
A:
It uses Vaporized Hydrogen Peroxide (VHP) technology to ensure efficient sterilization with a 99.9999% kill rate.
Q:Can the sterilization time be adjusted?
A:
Yes, the sterilization time is adjustable and typically ranges from 30 to 120 minutes.
Q:What materials are used for the VHP Pass Box?
A:
The box is made of high-quality stainless steel, available in SUS304 or SUS316 grades.
Q:How does the interlock system work?
A:
The double door interlock system ensures that only one door can be opened at any time to prevent cross-contamination.
Q:Is the device suitable for cleanroom environments?
A:
Yes, it is designed for Class A cleanrooms and is suitable for pharmaceuticals, laboratories, and electronics industries.
Send Inquiry
*To:
Suzhou Pharma Machinery Co., Ltd.
Suzhou Pharma Machinery Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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