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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
It is mainly used in pharmaceutical production to inspect impurities in ampoule injection. The inspect items includes impurities in which glass crumbs , fiber , hair , white powder, white dots are included and appearance inspect in which focal head, carbide, convex head, socket head and bubble head are included.
Working process
Products to be inspected→ infeed bottles→ bottle pressing→ rotate bottles → stop → take pictures → photoelectric inspection area → image processing software system analysis → bottle outfeed → Qualified bottles and the rejects collection
Main Structure
1. Rack → bottle-infeed conveying devices → bottle-infeed wheel→rotary tray→ bottle-pressing device → rotary apparatus → cam lift → quick change size parts device → outfeed wheel → qualified products/rejects collection plate.
2. Driving system、servo system → computer software processing system → control system
3. inspection camera → lighting device → light harrier → Light source servo tracking device → image processing system
Main technical parameters
1.Inspection speed: 600×(1±5%) pcs/min
2.Bottle: 1-5ml Ampoules
3.Total electric capacity: 5.9kW
4.Voltage: 380V，50 Hz
5.Precision: ≥40μm
6.Bench height: 900mm
7.Dimensions: 3530×1700×2000mm(L*W*H)
8.Net weight: about 1800kg
Main technical characteristics
1.Adopt seismic design , enables the machine to be more stable.
2.Use external electrical box layout to enhance the machine’s anti-interference ability
3.The key drive bearings use Sweden SKF and Japan NSK brand.
4.Screw bottle station brake is change to fixed location brake which enables the machine to be more stable and easy to maintain.
5.The up turntable is updated to integral lifting mechanism controlled by servo which makes it easier to adjust when change size parts
6.More than thirty patents are used in its designing.
7.The inspecting result is reliable. It accords with Europe pharmacopoeia and the Knapp regulation of prevailing FDA USA.
One year of qualification
Audited Supplier
Pharma Sources Insight January 2025
