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GMP Aseptic & High Containment Isolator, Custom Vhp Sterilization Wip Wash-in-Place, Removable
US$18,999.00-26,999.00
1 Piece

Product profile

Customization

Available

Application

Chemical Industry, Food Industry, Food Safety, Pharmaceutical Industry

Certification

GMP, ISO

Model NO.

isolator-2

Control System

Fully Automatic

Customized

Customized

Material

Stainless Steel

Pressure

-500PA

Standard

ISO10648-2

Door Seal

Silicone

Cleanliness

ISO 7

Air Change Per Hour

> 30 Ach

Airflow Type

Turbulent Flow

PLC

Siemens

Touch Screen

Siemens

Noise

≤60 Dba

Transport Package

Wooden Case

Specification

SS304

Trademark

KPL

Origin

China

Key features

Dual Working Modes: Switch between positive pressure for aseptic operations and negative pressure for toxic materials.
OEB5 Containment Performance: Ensures safe handling of highly potent compounds with 100% FAT testing compliance.
Customizable Layout: Modular design allows adding chambers to match specific production or laboratory processes.
Selectable Chamber Material: Choose between SUS304 and SUS316L stainless steel based on application needs.
Fully Welded Internal Chamber: Constructed from single-piece SS316L with coved corners for superior cleanability.
Automated Pressure Decay Test: Built-in integrity test verifies leak-tightness before every operation cycle.
Safe-Change HEPA Filter: Push-push design minimizes operator exposure during filter replacement.
GMP-Optimized Finishing: Low surface roughness interior and exterior facilitate easy cleaning and reduce particle retention.

Company profile

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2017-01-01Average Response Time: ≤8.73hTerms of Payment: LC, T/T, D/PInternational Commercial Terms(Incoterms): FOB, EXW, CIF, DAP, FCA

AI-Powered supplier vetting

SummaryKPL CONTROLLED ENVIRONMENT SOLUTION (SUZHOU) CO., LTD. is identified as a trading company involved in air filtration, contamination-control, personnel-protection, and related equipment and materials. The supplier reports six production lines, 6–10 quality-control staff, in-stock service capacity, and lead times within 15 workdays in both peak and off-season periods. It claims documented service-capability assessment and corrective/preventive-action procedures, as well as R&D activity, ODM services, and OEM experience for well-known brands. However, it has no overseas warehouse, showroom, agent, branch, or offline trade-show participation, and its overseas-service coverage is listed as zero countries. Financial records are indicated for 2022–2024, but no financial results are provided. The available customer evidence identifies NANOCLEAN TECHNOLOGIES, while the supplier registration date is August 2025.
After-Sales capabilityThe supplier reports written procedures and followed records for service-capability assessment and corrective/preventive actions, plus in-stock service capacity and lead times within 15 workdays during both peak and off-season periods. However, it has no overseas warehouse, showroom, agent, or branch, and lists service coverage in zero countries, limiting evidence of localized overseas after-sales support.
R&D capabilityThe supplier reports new products during the past year and offers ODM services, while its business scope includes R&D for air filtration and contamination-control equipment. It has no available SDK, so its innovation capability is supported for product development and design manufacturing but not for SDK-based integration.
Production capacityThe supplier reports six production lines, 6–10 quality-control staff, stated annual output information of 20,000 HEPA terminal boxes and 1,000 BIBO units, and lead times within 15 workdays in peak and off-peak periods. These figures support evidence of operational production capacity and delivery readiness, although the supplier is also classified as a trading company.
Customization capabilityThe supplier explicitly reports ODM availability and OEM service for well-known brands, indicating capability to support customized design and branded manufacturing. Its stated R&D scope further supports this conclusion for filtration and contamination-control products.

Product Q&A

Q:What containment level does this isolator provide?
A:
It delivers OEB5 containment performance, ideal for handling High Active Pharmaceutical Ingredients (HAPIs/HPAPIs) and cytotoxic drugs.
Q:Can the isolator operate in both positive and negative pressure?
A:
Yes, it features dual working modes: positive pressure for aseptic operations and negative pressure for toxic and hazardous materials.
Q:Is the chamber material customizable?
A:
Yes, the chamber material is optional and can be selected between SUS304 and SUS316L stainless steel.
Q:What is the standard configuration of the isolator?
A:
The standard configuration includes a main glove chamber and a pre-chamber, with additional modules available for customization.
Q:Does the system include automated testing?
A:
Yes, it is equipped with an automated pressure decay test that verifies leak-tightness and system readiness before each operation.

Send Inquiry

*To:Kpl Controlled Environment Solution (Suzhou) Co., Ltd.Kpl Controlled Environment Solution (Suzhou) Co., Ltd.
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