Negative-pressure Isolator

The negative-pressure isolator is often used for the weighing, dispensing, feeding and other operations of highly active, toxic and allergenic drugs. The operation process is isolated through the closed barrier system to protect the health of the operator. Its internal environment cleanliness is Class C and meets process and cGMP requirements. It is widely used in the fields of medical, pharmaceutical, chemical, food industries and so on.

Negative-pressure Isolator
Negative-pressure Isolator
Negative-pressure Isolator
Negative-pressure Isolator
  • Product Description
  • Technical Features
  • Technical Parameters
  • Optional Systems
  • Application Scenarios
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    1. High protection level: up to the highest OEB 5 (OEL<1ug/m³);

     

    1. Professional customization: according to different process requirements (explosion-proof function is optional), we provide the most suitable isolator design and complete MOCK-UP early in the design and three-dimensional display in the middle of a project.

     

    1. Intelligent: intelligent control system, a number of expansion ports, such as printing, storage, etc., and can be integrated into SCADA system;

     

    1. Perfect WIP system: the bottom of the chamber is designed to be inclined and the internal arc angle R20, without hard-to-clean places;

     

    1. Automatic regulation and emergency system: when leakage occurs, the isolator automatically gives an alarm and adjusts the fan frequency to ensure that the air speed of crack is greater than 0.5m/s.

     

    1. Various material transfer: configurable RTP (Rapid transfer ports) and online waste discharge port (bagging system);

     

    1. Safe filter replacement: PUSH-PUSH filters of the air handling system can be replaced safely to protect personnel’s safety.

     

    1. Real-time monitoring of door status: it can monitor the door opening online and continuously monitor the inflatable sealing of the door;

     

    1. CDCV service: sterilization cycle development, validation studies and services;

     

    1. High-quality manufacturing materials: the inner chamber is made of 316L or PTFE, and the chamber polishing grade is 0.4μm~0.6μm; the brands of all key components are international first-class such as Camfil, EBM, SIEMENS, etc.

     

     

     

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Full-process Consulting Services

Full-process Consulting Services

Whether you are preparing to build a new pharmaceutical factory, build a cleanroom that complies with local GMP regulations, or purchase pharmaceutical equipment to develop a new production line, whether it is a separate cleanroom or pharmaceutical machine project, or a one-stop solution, Marya's professional teams in the fields of pharmaceutical technical process, process equipment, decoration engineering, HVAC engineering, pipeline engineering, utility equipment, intelligent automatic control systems, project cost and other fields can provide you with full-process technical consulting services, and solve your needs one-on-one.

2D/3D Design Modeling Services

2D/3D Design Modeling Services

Marya project design team is composed of professional CAD and BIM engineers with more than 20 years of comprehensive industry experience and can provide you with comprehensive design services, including but not limited to process layout drawings, technical process charts, 3D models and animations, air conditioning system scheme design, construction drawing design, plant/pharmaceutical machine layout drawings, etc.

Machine Customization Services

Machine Customization Services

Based on the individual needs of clients in different countries, Marya helps you clarify specific needs, match appropriate models, and customize one stop filling solutions for sterile small-volume preparations, large-volume injections, oral liquids/syrups, solid preparations, etc.

Validation Services (FAT/SAT)

Validation Services (FAT/SAT)

Marya will appoint an engineer with rich project management experience as the person in charge, who will be fully responsible for project management and liaison work. After the equipment is manufactured, our engineers and the buyer's representatives will participate in the FAT test. After the equipment arrives at the buyer's site, it will be installed and debugged. After the equipment reaches optimal operation, the buyer will conduct SAT testing and inspection.

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