Product Description
GMP Modular Clean Room Ceiling Panel System A1 Fire Rated Sandwich Board Dustproof Certified
Purification engineering design Cleanroom Solutions
(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.
Clean Room Accessories We Can Supply
| Wall/ceiling panel |
Machine-made or Hand-made sandwich board |
| Clean room equipment |
Air shower, FFU, Pass box, Laminar flow cabinet hepa box |
| Cleanliness |
Class100-100000 |
| Purification system |
HVAC, Or AC conditioner+FFU |
| Floor |
PVC anti-static floor or epoxy-based coating |
| Other accessories |
salinity window, LED panel light, Door, Hand wash sink, storage/shoe cabinet, etc |
| Service |
Design, manufacturing, construction |
Clean Room Wall And Ceiling Panel Type
Product Parameters
Dust Free Clean Room are essential to any manufacturing process where particulate contamination can affect the quality of goods produced. Specific clean room classifications and ISO class code descriptions provide protective guidelines and secure environments through controlled air filtration, which lowers the possibility of product contamination or large particulate interference within critical process manufacturing. Specific cleanroom requirements and ISO 14644-1 cleanroom standards are used to protect consumers from any potential flaw or mishandling of a product.
Additionally, clean room classifications require that positive pressure is continuously maintained while the cleanroom is
operational. This process prevents contaminated air from flowing back within the clean air environment. This process allows clean filtered air to continuously flows from clean to less-clean spaces, allowing for continual air movement.
Audited Supplier 
){kind=link}