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GMP Isolator for Pharmaceutical Production Line
US$19,800.00
1 Piece

Product profile

Customization

Available

Certification

GS, CE, ISO9001

Noise

20-40db

Model NO.

PH-1200

Application

Industrial

Control Mode

Touch

Usage

Dust Removal, Smoke Removal, Adding Oxygen, Sterilization

Cleanliness

ISO 5-8

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

Vhp Residual Removal Efficiency

Less 1ppm

Control Method

Manual or Automatic

Cabin Material

External Full 304 Stainless Steel, Internal Cavity

Outer Dimension(W*D*H)mm

1600*880*2250

Operating Cabin Size(W*D*H)mm

1195*680*700

Transfer Cabin Size (W*D*H)mm

600*680*700

Power V/Kw

AC220 /3.5

Compressed Air Volume

0.5MPa

Illustrate

Single Double Cabin

Transport Package

Export Package

Specification

Custom request

Trademark

suzhou pharma machinery

Origin

China

HS Code

842489

Production Capacity

20sets/Month

Key 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

Suzhou Pharma Machinery Co., Ltd.
Experienced TeamImporters and ExportersHigh Repeat Buyers Choice
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.

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