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GMP Isolator for Pharmaceutical Production Line
US$19,800.00
1 Piece
Product profile
Customization
AvailableCertification
GS, CE, ISO9001Noise
20-40dbModel NO.
PH-1200Application
IndustrialControl Mode
TouchUsage
Dust Removal, Smoke Removal, Adding Oxygen, SterilizationCleanliness
ISO 5-8Leakage 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 HydrogenVhp 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 pharma machineryOrigin
ChinaHS Code
842489Production Capacity
20sets/MonthKey features
Safe Toxic Dust Handling: Bag-in-bag-out filtration system allows direct outdoor discharge of toxic substances.
High-Grade Stainless Steel: External made of 304 stainless steel; internal chamber crafted from 316L stainless steel.
Flexible Customization: Glove operation height and cabin configurations can be customized to working positions.
User-Friendly Operation: Equipped with touch screens and PLC control for safe operator interaction outside the isolator.
Multi-Stage Process Support: Designed for granulation, coating, tablet pressing, and blister packing in a single line.
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: ≤1.56h
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:How does the isolator handle toxic dust?
A:
It uses a bag-in-bag-out filter system that filters toxic substances and allows direct outdoor discharge, meeting safety requirements.
Q:What materials are used for the isolator construction?
A:
The external structure is made of full 304 stainless steel, while the internal cavity uses 316L stainless steel for high-grade corrosion resistance.
Q:Can the isolator height be customized?
A:
Yes, the height of the glove operation can be customized according to the machine's working position.
Q:What is the sterilization efficiency of the system?
A:
The system provides sterilization efficiency of 6lg with VHP residual removal efficiency of less than 1PPM.
Q:What are the available cabin configurations?
A:
Options include single person single cabin, single person double cabin, double person single cabin, and double person double cabin configurations.
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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