Active Member
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[China]
Address: Plant 106, No. 25, Taian Road, XINQIAO VILLAGE, PANYU DIST. GUANGZHOU CHINA
Contact name:VANESSA WANG
Guangzhou Anlai Airtech Co.,Ltd |
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Medical Device Cleanroom sulotions:
(1) It is crucial to maintain a contaminant-free clean environment when manufacturing medical devices such as biological implants. This starts with the cleanroom design and management systems. The cleanroom design prevents outside contamination, while regular maintenance and sanitation upkeep minimize the risk of contamination originating within the cleanroom itself.
(2) Implants that are non-sterile or are awaiting sterilization should be subject to purification and clean packaging processes. This will allow for uniformity and control over product quality. When constructing a GMP Medical Instrument Cleanroom, a location should be designated for the packaging process, and processes should be implemented to ensure that products avoid contamination risk at all times.
(3) Procedures must be developed to control environments in which there exists a contamination risk to products. This includes any time personnel makes contact with a product, including when products are moved from one location to another.
Application: E-Cigarette, LCM, CMOS Camera Module, Touch Play, Optical Module, FILM, Biological Pharmacy,
Packing,Food
Main Features
(1) Assembly structure designed, easy installation and easily moved
(2) Directional wheels can be installed, suitable for small
building and high cleanliness area;
(3) Modular design: clean booth can be as small as several square
meters and can be as large as hundreds of square meters
(4) It has large useful and effective area; while compared with
traditional clean room, it has such features like low investment,
high return and stable.
What We Can Do For You?
Front end consultancy support, Concept design and engineering.
Clean room design and construction.
Unique range of clean room modular walls and ceilings, flooring system.
Cleanroom accessories (pass boxes, step over benches, change room furniture and fittings, sampling and dispensing booths, air showers, etc.) GRP clean room doors.
Equipment selection ,Validation master plans, protocols and continuous monitoring systems regulatory advise.
HVAC Design and Installation.
