Oral Liquid Tamper-evident Cap Production Line

Model No.

KP-OL0311

Types Of

Core Selling Point

Compliant With Pharmaceutical Packaging Standards, Sterile & Clean, Easy Opening, Child Safety, Clear Traceability

Applicable Industry

Pharmaceutical Factories, Pharmaceutical Cap Manufacturers, Pharmaceutical Packaging Enterprises

Degree Of Automation

Fully Automatic

Voltage

380V

Standard Equipment Configuration

25T Punching Machine, Single-head Gasket Insertion Machine, Electromagnetic Induction Heating Sealing Equipment, Class 100,000 Clean Production Unit, Batch Number Printing Equipment

Core Components

PLC, Motor, Bearing, Pump, Clean Die, Electromagnetic Induction Heating Equipment

Power

26KW

Production Capacity

200 caps/min

Suitable Cap Size

Standard Sizes For Oral Liquid Bottles

Dimension(L×W×H)

7800×1200×1900mm

Weight

16T

Mechanical Test Report

Provided

Warranty Period

1Year

Certification

CE Certification, Relevant Pharmaceutical Packaging Certifications

Place Of Origin

Yantai, China

Brand Name

Kun Peng

Video Factory Inspection

Provided

After-sales Service Provided

Engineers Available To Service Machinery Overseas

Detailed Introduction

This production line is the key to safe pharmaceutical packaging, strictly complying with pharmaceutical packaging standards, producing aluminum-plastic composite easy-open caps (pull-ring caps/tear-off caps) and child-resistant caps (CR caps). The aluminum-plastic cap seals the aluminum foil with the bottle mouth through electromagnetic induction heating, and the pull-ring design is easy to open and leaves obvious traces; the child-resistant cap can only be opened with specific skills (pressing down while rotating), effectively preventing children from accidental ingestion.

The production line operates in a class 100,000 clean workshop and implements cGMP standards to ensure that the cap is clean and sterile, precise in size, reliable in sealing, and clearly printed with traceability information such as batch numbers. The product provides full-cycle safety guarantee for liquid drugs from production to consumption, and is an indispensable standardized component in the pharmaceutical industry, adapting to the strict quality requirements of the pharmaceutical industry.