Ai Intelligent Visual Inspection System Machine For Transparent Bottle Cap

The packaging of medicines is different from the packaging of general articles. The packaging of medicines is restricted by the inherent properties of the medicines, that is, the efficacy of the medicines must be maintained, safety and health, and the trust of the users must be maintained. This must fully prevent moisture absorption, air leakage and light caused by Decompose and deteriorate. Therefore, the packaging of medicines is a guarantee for maintaining the properties of medicines and the correct use of medicines.

Detection principle

Pour the bottle cap with a diameter of 5`6mm into the cap arrange equipment through the conveying line transport it stably and orderly through the photographing area of the industrial camera, and transfer the captured high-pixel sample image to the image processing software for comparison and analysis with the standardized model. After comparative analysis, it is determined whether the concave surface of the bottle cap, the trademark surface, and the side are defective, and the defective products are eliminated by compressed air, and the qualified products are finally collected

The standards are as follows :

The counting function can be realized after the finished product is tested, and the counting accuracy rate is 100%.

During use, the testing equipment needs to be maintained and cleaned regularly (such as conveyor belt cleaning, camera cleaning, etc.). The testing equipment itself will not cause secondary pollution sources (such as debris, fine foam, etc.) to the tested samples.

Software function:

Enabling and disabling the system detection function

Adjustment of detection index parameters and accuracy.

Camera screen calibration function

Real-time display system production information (qualification rate, total output, speed, etc.), browse historical production information, export and store functions. Template sampling and storage, sample detection information storage and recall.

Permission management of login accounts (such as general operation users disable parameter adjustment permissions)

Operation and adjustment of the mechanical part of the system

(Such as the transmission device is opened, the air valve injection time is adjusted, and the alarm signal is adjusted)

Significance of drug packaging:

Qualified drugs should have the characteristics of sealing, stability, lightness, beauty, appropriate specifications, standardized packaging, qualified, clear, etc., to meet the entire process of drug circulation, storage and user use.