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LGL 200 Pharmaceutical Fluidized Bed Granulator

LGL 200 Pharmaceutical 

Fluidized Bed Granulator


The equipment is very flexible in the production process of different products, according to different formulations and different application environments, convenient and fast switching.

▶Versatility ensures optimal product acquisition.

Easy to integrate with other pelleting equipment to meet customers' requirements for high automation.

The hopper is equipped with an air dispersing device with a screen to prevent the loss of drugs to the bottom of the machine.

Non-welding between the air dispersion device and the hopper facilitates disassembly and inspection after cleaning.

With the increasing demand for OEB3-5 powder treatment, granulation, tablet pressing, capsule filling and coating production and R&D equipment. SMA timely launch all kinds of high sealed solid preparation line, to meet the market needs.

The design of enclosed equipment must be a risk-based solution. Conduct a preliminary analysis of key and potential risks to the process and plant conditions in which the drug will be used, such as regulations, layout, and industrial objectives.

The αβ valve is fed with high-activity powder, and the closed chamber adopts pneumatic sealing ring, which will not be deflated after power failure to ensure complete sealing and isolation of the production area.

The closed chamber is made of stainless steel AISI304, which maintains a slight negative pressure during production.

The side door has the function of automatic locking and detection when the machine is turned on, so as to prevent operators from misoperation and causing injuries to personnel. Inflatable sealing ring is adopted.

The purified air passed through the junior high HEPA filter is sent to the main engine by the blower, and the exhaust air is filtered by the dust collector and the bag in bag out HEPA filter, and then discharged to the outdoor by the exhaust fan. During the whole production process, the micro-negative pressure of -50Pa is maintained in the host cavity. 

All parts that come into contact with the product will be wetted or subjected to a more rigorous and sophisticated online cleaning process based on an operational risk control analysis prior to removal.