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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
Applications
It’s mainly used for the automatic inspection of the visible impurity (such as glass or metal scraps, fiber, hair, and white powder or flakes) in ampoule injection and the liquid level. It can be also used for the visible impurity in vials and oral liquid bottles.
Principle
Use mechanical visual principle to take an identification inspection on the visible impurity. The product is held stopped to a standstill while it rotates at a high speed. At that moment, an industrial camera takes a series of pictures continuously on it. These pictures are analyzed and compared by a compute system to judge whether the inspected product is qualified, meanwhile divide them automatically into the qualified and the rejects.
Inspecting procedure:
Products to be inspected → feed in → enter the photoelectric inspection zone → rotate the bottle → stop → take pictures → the bottles dividing device distinguishes the qualified bottles and the rejects according to the software instruction → the qualified bottles and the rejects feed out separately
Specifications:
1 Application range: 1 ml to 20 ml ampoules, vials and oral liquid bottles.
2 Inspecting items: visible impurity ((suck as glass or metal scraps, fiber, hair, and white powder or flakes) and the liquid level.
3 Inspecting speed: 150 pcs/ min (1±5%)
4 Inspecting precision: ≥40μm（adjustable）
5 Power：3kW
6 Voltage： AC380V 50Hz
7 The Height of working table: 900mm
8 Overall dimensions: 2980mm×1300mm×1650mm（ L×W×H）
9 Net weight: about 1200kg
Advantages
Passed the appraisal of the state science and technology achievement,it fills the domestic gap, substitutes the import product and reached the international advanced level.
Adopt technologies of more than 20 inventions and utility model patents.
The inspecting result is reliable. It accords with European pharmacopoeia and the Knapp regulation prevailing in FDA.
Run smoothly with low breakage rate.
Inspecting precision is adjustable, and accords with the production demand.
Easy and quick to change the size parts.
The inspection data of a certain period can be reserved, which is convenient for quality analysis. It can be connected with a printer.
One year of qualification
Audited Supplier
Pharma Sources Insight JANUARY 2024
