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Email ：PharmaSources@imsinoexpo.com
Whatsapp ：+86-13621645194
Main Sales Markets: North America,Central/South America,Western Europe,Eastern Europe,Australasia,Asia,Middle East,Africa
Sample Provided: no
Product details
Used in pharmaceutical factory production to automatically check impurities in plastic bottles infusion. Inspected items includes: glass crumbs, hair, white powder etc and liquid level. Inspect scope: 50ml-250ml infusion in plastic bottle and glass bottle.
Technical parameters
1. Inspection speed: 0- 300 pcs/min
2. Bottle: 50ml-250ml plastic infusion bottle and glass bottle
3. Precision: ≥40μm
4. Electric capacity: 10kW
5. Voltage: 380V，50 Hz
6. Compressed air: 0.8MPa
7. Bench height: 900mm
8. Dimensions: 4600×2450×2300mm(L*W*H)
9. Net weight: about 3000kg
Working principle
Bottle conveying rail containers will be sent to the bottle into the bottle feeding screw. Bottle feeding screw transfer the detect bottle to the feeding wheel, a bottle feeding wheel will transport the container to bottle-rotating mechanism on the turntable. Impurities like glass crumbs, hair and white powder will rotate at high speedin the container. when the container reachthe inspection station, the container will stop rotating by the brake mechanism as soon as it reach the station, three groups of industrial camera in the tracking detection mechanism take multi-frame photographs, then the industrial computer can judge whether there are impurities in the detection containers by analyzing multi frame picture, When impurities in the container are checked out, bottle distribution servo motor will finish the waste reject action according to the program instructions, making qualified products and defective products separate from each other.
Equipment characteristics
1. The whole machine absorbed many advanced foreign technology and through innovative research and development, It has completely independent intellectual property rights;
2. The machine has compact structure, simple design, convenient maintenance and strong commonality.
3. Inspect mechanism is placed above working table, full comply with GMP requirements.
4. Inspecting precision is adjustable to meet different requirements of customers.
5. Inspect data can be obtained, stored and printed out, which ensure the process parameters to be traced, which is in line with GMP requirements.
6. The key components (like cameras, light source, servo motor, main motor, the inverter, switch, controller, drive bearing and sliding bearing etc. ) of machine use the Imported or well-known brand of china.
7. Adopt European pharmacopoeia and American FDA acknowledged Knapp test procedure, to make the detection of the main functions and parameters to be verified, and conform to the requirements of the industry internationalization.
One year of qualification
Audited Supplier
Pharma Sources Insight June 2024: Globalization on the Go
