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Positive Pressure Compounding Aseptic Sterile Isolator Laminar Flow ISO Requirement Isolator
US$10,000.00
1 Piece
Product profile
Customization
AvailableCertification
CENoise
60-70dbApplication
IndustrialControl Mode
TouchUsage
Humidification, SterilizationCleanliness
ISO Class 5Leakage Rate
Less 0.5%Vol/H (Under 100PA)The Number of Air Changes
More Than 80t/HVaporization Temperature
Less 80 CCompressed Air
0.3-0.5MPaSterilizer
Better Than 30% Food Grade Hydrogen Peroxide SolutVhp Residual Removal Efficiency
Less 1ppmControl Method
Manual or AutomaticCabin Material
External Full 304 Stainless Steel, Internal CavityOuter Dimension(W*D*H)mm
1600*880*2250Operating Cabin Size(W*D*H)mm
1195*680*700Transfer Cabin Size (W*D*H)mm
600*680*700Power V/Kw
AC220 /3.5Compressed Air Volume
0.5MPaIllustrate
Single Double CabinTransport Package
Export PackageSpecification
Custom RequestTrademark
SUZHOU PHARMAOrigin
ChinaProduction Capacity
100 Sets/MonthKey features
ISO Class 5 Cleanliness: Maintains ISO Class 5 cleanliness level for aseptic operations.
Advanced Leak Detection: Automatic inflation and sealing check ensures airtight requirements before sterilization.
Efficient Flash Evaporation: High-precision temperature control ensures 100% hydrogen peroxide vaporization.
Rapid Residue Removal: Configured decomposer rapidly removes hydrogen peroxide from space and surfaces.
304/316L Stainless Steel: External 304 and internal 316L stainless steel for superior corrosion resistance.
Computerized Verification: Includes audit trail, electronic signature, and data integrity features.
Door Interlock Safety: Door remains locked during equipment operation to prevent contamination.
Bacteriostatic Surface: Interior treated to prevent microbial hiding and ensure sterility.
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: ≤2.02h
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 is the cleanliness standard of the isolator?
A:
The isolator meets ISO Class 5 cleanliness requirements.
Q:How does the leak detection system work?
A:
It automatically inflates the cabin to check for airtightness. If requirements are not met, it continues inflating and sealing until the conditions are satisfied.
Q:What sterilization method is used?
A:
It uses an efficient flash evaporation method with better than 30% food grade hydrogen peroxide solution.
Q:What materials are used for the cabin construction?
A:
The exterior is made of full 304 stainless steel, and the internal cavity is made of 316L stainless steel.
Q:Does the system support data integrity features?
A:
Yes, it conforms to computerized verification software with audit trail, electronic signature, and data integrity functions.
Send Inquiry
*To:
Suzhou Pharma Machinery Co., Ltd.
Suzhou Pharma Machinery Co., Ltd.*Content:
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