What is the leakage rate of the system?

The leakage rate is less than or equal to 0.5% VOL/h at pressures below 100pa.

What is the minimum order quantity?

The minimum order quantity is 1 set.

CE Certified Aseptic Inspection Isolator for Sterile Pharmaceutical Packaging Defect Detection

Name: CE Certified Aseptic Inspection Isolator for Sterile Pharmaceutical Packaging Defect Detection
Brand: Suzhou Pharma Machinery Co., Ltd.
SKU: 1920914696

Jiangsu, ChinaSuzhou Pharma Machinery Co., Ltd.

US$19,800.00

1 Piece

Product profile

Customization

Available

Certification

CE, ISO9001

Noise

60-70db

Application

Industrial

Control Mode

Touch

Usage

Dust Removal, Sterilization

Transport Package

Export Wooden Case

Specification

Customized

Trademark

suzhou pharma machinery

Origin

Jiangsu

Key features

CE and ISO9001 Certified: Meets international safety and quality standards for pharmaceutical equipment.

100% Hydrogen Peroxide Steam: High-precision system ensures zero decomposition during evaporation.

Rapid Residue Removal: Decomposer quickly eliminates both spatial and surface hydrogen peroxide residues.

Automatic Sterilization Recording: Automatically detects concentration and generates sterilization process curves.

Door Interlock Safety: Equipment doors remain locked during operation to ensure safety.

Antibacterial Interior Surface: Permanently free of microbial habitats with specialized antibacterial treatment.

Compliant Verification Software: Includes audit tracking, electronic signatures, and data integrity functions.

Customization Available: Offers full customization, flexible customization, and customization from samples.

Company profile

Experienced TeamImporters and ExportersHigh Repeat Buyers Choice

Suzhou Pharma Machinery Co., Ltd.

Jiangsu, China

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 certifications does the isolator have?

The equipment is certified with CE and ISO9001 standards.

Q:How does the sterilization process work?

It uses an efficient flash evaporation method ensuring 100% hydrogen peroxide forms steam with zero decomposition.

Q:Can the system record sterilization data?

Yes, it automatically detects sterilization concentration and draws sterilization process curves.

Q:Is the interior surface antibacterial?

Yes, the interior surface adopts antibacterial treatment to remain permanently free of microbial habitats.

Q:What materials are used for construction?

The exterior is made of 304 stainless steel and the internal chamber is 316L stainless steel.

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CE Certified Aseptic Inspection Isolator for Sterile Pharmaceutical Packaging Defect Detection