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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: ≤4.22h
About Our Factory & Business Background
AddressNo211, North Fute Road, Pudong Area, 200131, Shanghai, China
Plant Area3210 square meters
Number of Employees69
Terms of PaymentLC, T/T, D/P, PayPal, Western Union, Small-amount payment, Money Gram
International Commercial Terms(Incoterms)FOB, EXW, CFR, CIF, DDP, CIP, Others
Average Lead TimePeak Season Lead Time: 1-3 months Off Season Lead Time: one month
Minimum Order Quantity1 Set
Supply Chain Partners150
Our Production Capability & Technical Expertise
Main ProductsPharmaceutical Filling Line, Cleanroom Project
Production Lines6
Production MachinesWelding Machine, Lathe, Milling Machine, Bench Drill
QA/QC inspectors3 people
Inspection Type for Finished Products100% inspection(Visual inspection & Function inspection)
Inspection Method for Finished ProductsHave instructions and uniformly followed
R&D Engineers30 people
Traceability of Raw MaterialsYes
Our Industry Experience & Global Business Record
Year of Establishment2014-03-10
Main MarketsNorth America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, Western Europe
Repeat Buyers Choice10%~30%
Number of Foreign Trading Staff16
Overseas Agent/BranchNo
New Products Launched in Last yearYes
Our Certifications, Standards & Industry Recognition
Product CertificationCE
Cooperated with Fortune 500Yes
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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