Advanced Sterile Negative Pressure Inspection Isolator System for Maximum Protection

Customization: Available
Certification: GS, RoHS, CE, ISO9001
Noise: 60-70db

Product Description

Basic Information

Model NO. M-ISLT-N
Application Industrial
Control Mode Touch
Usage Fragrance, Dust Removal, Smoke Removal, Humidification, Formaldehyde Formaldehyde, Adding Oxygen, Sterilization
Inlet Air Speed 0.45m/S±20%
Rated Power 4.2kw
Indoor Illuminance High Than 500 Lux
Control Operation PLC
Airflow Mode Turbulence
Package Size 2000.00cm * 2000.00cm * 2000.00cm
Package Gross Weight 1000.000kg
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Product Description

Negative pressure isolator M-ISLT-N
It can meet the isolation operation of highly toxic, highly active, and highly allergenic drugs, comply with the requirements of EHS occupational health management system, and can be widely used in laboratories related to biomedicine, chemical engineering, and research institutes. Provide a sealed negative pressure environment for the packaging, weighing, ingredient preparation, sampling and other operational processes of drugs, to protect the health and safety of personnel throughout the entire operation process.
Negative Pressure Inspection Isolator

Product Parameters

Model M-ISLT-01
External dimensions 3000 × 850 × 2200 mm
Noise ≤75 dB
Illuminance ≥ 300 LUX
Airflow mode Turbulence
Operating cabin pressure -100Pa ~ -20Pa
Power supply AC 220V, 50Hz
Protection level OEB 4
Cabin airtightness Meet ISO10648-2 standard requirements
HEPA filter PUSH-PUSH filter
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Detailed Photos & Advantages

  • SUS304 stainless steel production, customizable according to process requirements, negative pressure design;
  • Provide flexible, high-quality, and high safety isolation and sealing operation plans for personnel, materials, environment, and equipment involved in the production of highly toxic, active drugs, hormone drugs, and API products;
  • Optional water gun, air gun, etc. can be used to clean the cavity;
  • C-RABS and ISOLATOR options available; biosafety leakage level can reach OEB-4;
  • RTP technology, AB valve group, or transfer window form for material entry and exit;
  • Configurable bag in bag out system.
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Certifications & Production

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Profile & Exhibitions

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Packaging & Shipping

Why Choose Us?

  • Well-experienced: Founded in 2010. Focused on the pharmaceutical and chemical industry for over a decade.
  • Strong processing ability: Independent research and development, production base, and more than 20 advanced processing equipment.
  • Emphasis on R&D: Focuses on product research and innovation, with over ten R&D personnel and more than thirty patent certificates.
  • Complete verification: Comprehensive verification system with a dedicated team, complete materials, and after-sales service.
  • Professional: Deeply familiar with pharmaceutical production processes and verification system concepts.

FAQ

Q1: Are you a manufacturer? Ans: Yes, we have been manufacturing and providing excellent cleanroom and solid preparation front-end processing systems for more than 10 years. Our production plants are qualified for ISO Quality Management System.
Q2: Do you inspect the finished products? Ans: Yes, we conduct inspections according to ISO standards, managed by our dedicated QC staff.
Q3: Do you do OEM or ODM? Ans: Yes, we provide both OEM and ODM services. Custom logos can be applied to our products.
Q4: How long is the delivery time? Ans: Normally 7 days for standard samples. For customized orders, the lead time is approximately 60 days.
Q5: How long is the warranty period? Ans: One year after shipment.
Q6: What standards does the cabin airtightness meet? Ans: The cabin airtightness meets ISO10648-2 standard requirements.

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