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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's mainly used for the automatic inspection of the visible impurity (such as glass or metal scraps, fiber,hair, and white powder or flakes) and the liquid level in oral liquid, lt can also be used for Impurity inspection in vials.
Principle
Use mechanical visual principle to take an identification inspection on the visible impurity. The product is stopped to a stand still 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
Application rang：10ml to 20ml oral liquid.
Inspecting items：visible impurity (such as glass or metal scraps, fiber, hair, and white powder or flakes), liquid level and capping condition.
Inspecting speed： ADJ10－20/300B 300pcs/min（1±5%）
ADJ10－20/400B 400pcs/min（1±5%）
Inspecting precision： ≥40μm (adjustable)
Power： 5.5kW
Voltage： AC380V 50Hz
The Height of working table：900mm
Overall dimensions：3230×1700×2000mm（L×W×H）
Net weight：about1800kg
Main technical characteristics
Passed the appraisal of the state science and technology achievement it fills the domestic gap substitutes the import product and reaches the international advanced level.
Win the national invention Patent and adopted more than 30 Patented technology.
The inspecting result is reliable lt accords with European pharmacopoeia and the Knapp regulation prevailing in FDA
Run smoothly with low breakage rate.
lnspecting 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 convention for quality analysis, lt can be connected with a printer.
One year of qualification
Audited Supplier
Pharma Sources Insight JANUARY 2024
