Skip to main content

Comprehensive Medical Device Packaging Testing with Labthink Tensile Tester


The pharmaceutical and medical device industries demand rigorous quality control to ensure product safety and efficacy. One of the critical aspects of this process is comprehensive testing, which can be challenging due to the diversity of products and evolving regulatory standards. To address these challenges, Labthink has introduced C610H Auto Tensile Tester, a versatile instrument designed for efficient and accurate testing.


The C610H employs a range of test methods to evaluate the mechanical properties of various packaging components. These tests are essential for ensuring product integrity, safety, and performance.

  • žPiercing force measurement: Assessing the resistance of rubber stoppers and syringe needles to penetration.

  • žBreaking force determination: Evaluating the strength of ampoules.

  • žSeal integrity testing: Assessing the sealability of flexible plastic containers under external pressure.

  •  Combination force measurement: Evaluating the force required to connect syringe barrels and needle hubs.

  • žUnmating force measurement: Determining the force needed to separate needle shields.

  • žSliding performance evaluation: Assessing the friction and movement of plug stoppers and dovetail components



C610H is designed to accommodate a wide range of materials, including rubber, plastic, and glass. Its versatility allows for testing various packaging components, such as syringes, needles, ampoules, rubber stoppers, and flexible pouches.


By combining multiple testing functions into a single instrument, the C610H significantly reduces testing time and costs. Its user-friendly software provides real-time data, analysis, and reporting capabilities, enhancing efficiency and data management. Additionally, the instrument's safety features protect operators from potential hazards associated with testing certain products.

In conclusion, the Labthink C610H Auto Tensile Tester offers a comprehensive and efficient solution for testing pharmaceutical packaging and medical devices. Its versatile design, combined with accurate test methods, makes it an invaluable tool for ensuring product quality and compliance with regulatory standards.

As the demand for functional packaging materials grows, testing methods are evolving to ensure a more comprehensive evaluation of packaging films. Labthink encourages collaboration with packaging industry companies for quality control! Visit the website www.labthink.com to learn more!

Comments

Popular posts from this blog

Moisture Resistance Testing of Thermal Conductive Silica Gel Pads

Thermal conductive silica gel pads, crucial components in electronic devices, require effective moisture resistance to ensure optimal performance and longevity. This article delves into a comprehensive testing method for evaluating the water vapor transmission rate (WVTR) of these pads. Electronic components are sensitive to moisture, which can lead to corrosion, short circuits, and reduced reliability. Thermal conductive silica gel pads, often used to facilitate heat dissipation between electronic chips and radiators, play a vital role in preventing moisture ingress. Their moisture resistance properties directly impact the protection of sensitive internal components. The electrolytic sensor method, a widely recognized standard, is employed to measure the WVTR of thermal conductive silica gel pads. This technique involves creating a controlled environment with a high humidity chamber on one side and a low humidity chamber on the other. A sample of the thermal conductive silica gel pad ...

Quality Requirements of Lithium Ion Battery Separators

Business Challenge Lithium-ion batteries have one of the best energy-to-weight ratios, no memory effect, and a slow loss of charge when not in use. This makes them one of the most popular types of batteries for portable consumer electronics in today’s marketplace. Lithium-ion batteries can be found in cameras, laptops, power tools, toys and more. However, as recent well-publicized recalls demonstrate, they can pose a risk of fire and overheating. In addition, they can suffer from a reduced lifespan if not properly treated. As a result, new and stricter requirements are being implemented globally to address potential hazards, leaving manufacturers and purchasers of products containing lithium-ion batteries to meet increasing requirements and overcome safety concerns. Lithium Ion Battery Separators A Lithium Ion battery Separator is a permeable membrane placed between the anode and cathode of a battery. The main function of a separator is to keep the positive and negative electr...

Introducing Vacuum Decay Testing Method for Pharmaceutical Packaging Integrity

Maintaining the integrity of pharmaceutical packaging is fundamentally essential for safeguarding product efficacy and patient safety, and vacuum decay testing stands as a highly reliable non-destructive method for verifying this integrity. This technique, particularly effective for blister packs, vials, and pre-filled syringes, identifies leaks without compromising product sterility or efficacy. Vacuum decay testing leverages the principle that a sealed package, when subjected to a vacuum, will exhibit predictable pressure changes if it's leak-free. Conversely, a leaking package will show a different pressure profile. Specific Vacuum Decay Techniques:   Differential Pressure Transducers: These precise sensors measure the difference in pressure between the vacuum chamber and a reference chamber. This allows for detection of very small leaks. Absolute Pressure Sensors: These sensors measure the absolute pressure within the vacuum chamber, providing data to determine the rate of pres...