Can the product be customized?

Yes, we offer full customization, customization from samples, and flexible customization options.

What is the minimum order quantity?

The minimum order quantity is 1 set.

What are the lead times for delivery?

The average lead time is one month for both peak season and off-season.

Full Stainless Steel Negative Pressure Isolator Aseptic ISO5 for Chemical Cleanroom

Name: Full Stainless Steel Negative Pressure Isolator Aseptic ISO5 for Chemical Cleanroom
Brand: Suzhou Pharma Machinery Co., Ltd.
SKU: 2008105352

Jiangsu, ChinaSuzhou Pharma Machinery Co., Ltd.

US$5,000.00-10,000.00

1 Set

Product profile

Customization

Available

Certification

CE, ISO9001

Cleanliness

ISO Class 5

Model NO.

PH-500

Leakage Rate

Less 0.5%Vol/H (Under 100PA)

The Number of Air Changes

More Than 80t/H

Vaporization Temperature

Less 80 C

Compressed Air

0.3-0.5MPa

Sterilizer

Better Than 30% Food Grade Hydrogen Peroxide Solut

Vhp Residual Removal Efficiency

Less 1ppm

Control Method

Manual or Automatic

Cabin Material

External Full 304 Stainless Steel, Internal Cavity

Outer Dimension(WDH)mm

1600*880*2250

Operating Cabin Size(WDH)mm

1195*680*700

Transfer Cabin Size (WDH)mm

600*680*700

Power V/Kw

AC220 /3.5

Compressed Air Volume

0.5MPa

Illustrate

Single Double Cabin

Transport Package

Export Package

Specification

customized design

Trademark

SUZHOU PHARMA

Origin

China

Production Capacity

100 Sets/Month

Key features

ISO Class 5 Cleanliness: Maintains a controlled micro-environment meeting ISO Class 5 standards for sterile operations.

Advanced VHP Sterilization: Equipped with hydrogen peroxide vaporizer achieving >30% solution efficiency and <1ppm residual removal.

Automatic Leak Detection: System automatically inflates and seals until airtight conditions are met before starting sterilization.

304/316L Stainless Steel: External body uses 304 stainless steel while internal cavity utilizes 316L stainless steel for corrosion resistance.

Bacteriostatic Surface Treatment: Interior surfaces treated to prevent microbial growth, ensuring no hiding places for bacteria.

Computerized Verification Software: Features audit trails, electronic signatures, and data integrity compliance for pharmaceutical standards.

Door Interlock Safety: Safety mechanism prevents door opening during equipment operation to maintain sterile environment.

Flexible Customization Options: Offers full customization, sample-based customization, and flexible options for specific requirements.

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: ≤0.73h

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 level of the isolator?

The isolator maintains a cleanliness level of ISO Class 5, suitable for sterile isolation operations.

Q:How does the leak detection system work?

The system automatically inflates the cabin and checks for airtightness. It repeats the process until airtight conditions are met before starting sterilization.

Q:What sterilization method is used?

It uses an efficient flash evaporation method with hydrogen peroxide, achieving vaporization at 100% and residue removal efficiency of less than 1ppm.

Q:What materials are used for the cabin construction?

The external body is made of full 304 stainless steel, and the internal cavity is constructed from 316L stainless steel.

Q:Is the system compliant with computerized verification standards?

Yes, the system includes software with audit trail, electronic signature, and data integrity functions.