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Marya Aseptic Vhp Transfer Chamber Pass Box for Sensitive Pharmaceutical Sterilization
US$600.00
1 Piece
US$550.00
2+ Pieces
Product profile
Customization
AvailableOptional Accessory
Timer Switch, Intercom, Sterilization Lamp, FloodlightNoise
0-20dbModel NO.
MARYA AASurface Treatment
Baking FinishInside Diameter
800*800*800mmInstallation
Embedded TypeOperating Principle
LaminarType
Self-CleaningWhole Power
0.35kwPower Supply
220V/50HzEfficiency
H14, 99.995%Cleanliness Level
ISO 8Dimension
CustomizedLaminar Flow
70%Exhaust
30%HEPA
H14Main Body Material
Galvanized Steel with Powder CoatedWork Surface
304 SsUV Light
EquippedUV Control Programes
EquippedLight Intensity
800luxFront Window Glass
TemperedAutomatic Alarm
EquippedTransport Package
Export Wooden PackageSpecification
Standard/customizedTrademark
MaryaOrigin
ChinaHS Code
8409919100Production Capacity
5000pieces/YearKey features
VHP Sterilization Technology: Utilizes vaporized hydrogen peroxide to effectively kill fungi, bacteria, spores, and viruses.
GMP Compliance: Design and operation fully compliant with the latest GMP regulations for pharmaceutical safety.
Low-Temperature Protection: Suitable for temperature-sensitive products with no damage to materials during sterilization.
Ultra-Low Residuals: Ensures VHP residual level below 1ppm for safe and non-toxic material handling.
H14 HEPA Filtration: Prevents secondary contamination with high-efficiency filtration during decontamination phases.
Fast Cycle Time: Room temperature sterilization cycle completes in under 120 minutes.
Modular Design: Rounded vertical design with modular components for easy on-site assembly.
Customizable Dimensions: Dimension is fully customized to meet specific project requirements.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Full Customization, Flexible customization CertifiedExport Year: 12 Years CertifiedNearest Port: Shanghai Port; Ningbo PortAverage Response Time: ≤3.01h
AI-Powered supplier vetting
SummaryThe supplier, Marya, is a combined type company with extensive experience in pharmaceutical and medical industries. It lacks certain service capabilities, such as effective after-sales service and overseas infrastructure. While it excels in customization and maintains strong R&D capabilities, it does not introduce new products frequently. The company has significant export trade capacity, but lacks formal contracts and warehouse facilities.
Supplier typeThe supplier is described as a combined type company with three factories and extensive experience in the pharmaceutical and medical industries.
CertificationsThe company has expertise in securing GMP and FDA certifications for factory construction.
After-Sales capabilityThe supplier lacks written procedures or records for corrective and preventive actions, as well as for handling customer complaints.
Production capacityThe supplier lacks valid contracts for manufacturing capacity and has no in-stock service capacity.
Customization capabilityThe supplier offers full and flexible customization in design services.
Client casesThe supplier has a proven track record since 2014, maintaining relationships with major pharmaceutical companies such as Novartis and Novo Nordisk.
Product Q&A
Q:What sterilization method does the pass box use?
A:
It utilizes vaporized hydrogen peroxide (VHP) to effectively kill a broad spectrum of microorganisms including fungi, bacteria, spores, and viruses.
Q:Is the sterilization process safe for temperature-sensitive products?
A:
Yes, it is designed for low-temperature sterilization at room temperature, ensuring no damage to temperature-sensitive materials.
Q:What is the cycle time for sterilization?
A:
The room temperature sterilization cycle is less than 120 minutes, verified based on material bioburden and loading.
Q:Does the system meet GMP regulations?
A:
Yes, the design and operation of the VHP Sterilization Transfer Window are fully compliant with the latest GMP regulations.
Q:What is the VHP residual level after the cycle?
A:
The system ensures a VHP residual level of less than 1ppm, determined by process requirements.
Send Inquiry
*To:
Shanghai Marya Pharmaceutical Engineering & Project Co., Ltd.
Shanghai Marya Pharmaceutical Engineering & Project Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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