Disposable syringes are a fundamental component in modern healthcare, ensuring safe and hygienic injection procedures. Their quality, integrity, and functionality are crucial, as any compromise can lead to serious health risks for patients. Temperature and humidity are two environmental factors that can significantly impact the properties of disposable syringes, from the flexibility of the plastic components to the sterility of the contents. Our high - precision medical temperature humidity test chamber for disposable syringes is a specialized solution designed to meet the stringent testing requirements of the medical industry. This advanced chamber enables manufacturers, quality control professionals, and researchers to subject disposable syringes to precisely controlled temperature and humidity conditions, ensuring their reliability and safety.
The core strength of this test chamber lies in its ability to achieve ultra - high precision in temperature and humidity control. The temperature can be adjusted within a broad range, typically from -70°C to 150°C, with an astonishing precision of ±0.1°C. Humidity levels can be precisely regulated from 10% to 90% relative humidity (RH), with a precision of ±2% RH. This level of accuracy is essential for mimicking the diverse environmental conditions that disposable syringes may encounter during storage, transportation, and use. Whether it's the cool storage conditions in a pharmacy or the warmer, more humid environment in a tropical clinic, the chamber can replicate these scenarios with unparalleled precision.
To meet the diverse testing needs of disposable syringes, the test chamber offers a wide variety of customizable test profiles. Users can create complex, multi - stage test sequences that simulate the actual environmental changes a syringe will experience throughout its lifecycle. For example, a test profile could include rapid temperature changes to mimic the transition from a cold storage facility to a warm patient room, or cyclic humidity variations to simulate the effects of different storage conditions. These custom - programmed test scenarios allow for a more comprehensive evaluation of syringe performance under realistic conditions.
The test chamber is designed with a large - volume interior to accommodate a significant number of disposable syringes simultaneously. This is particularly beneficial for manufacturers conducting batch testing, as it allows for efficient and representative sampling. The interior layout is optimized to ensure proper air circulation around the syringes, enabling uniform exposure to the controlled temperature and humidity conditions. This high - volume capacity not only increases testing efficiency but also reduces the overall cost per unit tested.
A sophisticated monitoring and data logging system is integrated into the test chamber. Multiple sensors are strategically placed throughout the chamber to continuously monitor temperature, humidity, and other relevant parameters. The data is logged at high frequencies, providing a detailed and continuous record of the syringe's environment during the test. This data can be analyzed in real - time or retrieved later for in - depth post - test analysis. The comprehensive data logging capabilities allow for the identification of potential weaknesses in the syringe's design and performance, enabling manufacturers to make informed improvements.
Given the medical nature of disposable syringes, the test chamber is constructed using materials that are not only durable but also compatible with the syringes and their contents. The interior is made of non - reactive, easy - to - clean materials that do not release harmful substances or contaminants. This ensures that the test environment remains hygienic and does not affect the integrity of the syringes. Additionally, the chamber is equipped with air filtration and purification systems to maintain a clean and sterile environment during testing.
Safety is of utmost importance in the testing of disposable syringes. The test chamber is equipped with a comprehensive set of safety features, including over - temperature and over - humidity protection, fire suppression systems, and emergency stop buttons. In case of any abnormal conditions, such as a sudden increase in temperature or humidity, the safety systems will automatically activate to protect the syringes, the testing equipment, and the personnel. These safety features ensure a secure testing environment for all involved.
| Model | THC-225 | THC-408 | THC-800 | THC-1000 |
| Inside dimension(W x D x H) mm | 50 x 75 x 60 | 60 x 85 x 80 | 100 x 100 x 80 | 100 x 100 x 100 |
| Outside dimension(W x D x H) mm | 75 x 165 x 170 | 85 x 175 x 190 | 125 x 190 x 190 | 125 x 190 x 210 |
| Internal material | #304 Stainless Steel |
| External material | Powder coated #304 Stainless Steel |
| Temperature range | + 150℃~ - 70 ℃ |
| Humidity range | 5% ~ 98% R. H |
| Temperature resolution ℃ | 0.01 |
| Humidity resolution % R. H. | 0.1 |
| Temperature stability ℃ | ±0.3 |
| Humidity stability % R. H. | ±2 |
| High temperature ℃ | 100 | 100 | 100 | 100 |
| Heating time (min) | 20 | 30 | 30 | 30 |
| Low temperature | 0, -40, -70 | 0, -40, -70 | 0, -40, -70 | 0, -40, -70 |
| Cooling time (min) | 20, 50, 70 | 20, 50, 70 | 20, 50, 70 | 20, 50, 70 |
| Air circulation system | Mechanical convection system |
| Cooling system | Imported compressor, fin evaporator, gas condenser |
| Heating system | Sus304 Stainless steel High-speed heater |
| Humidification system | Steam Generator |
| Humidification water supply | Reservoir, Sensor-controller solenoid valve, recovery-recycle system |
| Controller | Touch panel |
| Electrical power requirements | Please contact us for requirements of specific models |
| Safety device | Circuit system load protection, compressor load protection, control system load protection, humidifier load protection, overtemperature load protection, fault warning light |
By subjecting disposable syringes to precisely controlled temperature and humidity conditions, manufacturers can identify and address potential quality issues early in the production process. This allows for the optimization of syringe design, materials selection, and manufacturing processes to ensure maximum quality and reliability. The ability to simulate real - world scenarios helps in improving the syringe's performance, such as the smoothness of the plunger movement and the integrity of the needle attachment, resulting in a safer and more efficient product for patients.
Testing disposable syringes in a controlled environment helps manufacturers evaluate the durability of different components and materials. The chamber's ability to replicate extreme temperature and humidity conditions allows for the identification of parts that may be prone to degradation, such as the plastic barrel becoming brittle or the rubber plunger losing its elasticity. By addressing these issues before mass production, manufacturers can improve the long - term durability of their syringes, reducing the risk of failure during use.
The medical device industry is subject to strict international and national regulations regarding the safety and quality of disposable syringes. Our high - precision test chamber enables manufacturers to conduct the necessary tests to ensure compliance with these regulations. By providing accurate and reliable test data, manufacturers can obtain the required certifications and approvals, facilitating the sale of their syringes in different markets around the world.
Early detection of potential problems through comprehensive testing in the test chamber can save manufacturers significant costs. By identifying and fixing issues before mass production, manufacturers can avoid costly product recalls, warranty claims, and customer dissatisfaction. The high - volume capacity of the test chamber also allows for more efficient testing, reducing the overall cost per unit tested. Additionally, the ability to optimize the syringe's design based on test results can lead to cost savings in terms of materials and manufacturing processes.
For research and development teams in the medical device industry, the test chamber provides a valuable tool for exploring new technologies and materials for disposable syringes. The ability to precisely control the temperature and humidity allows for in - depth studies of how these factors affect the performance of new materials, such as biodegradable plastics or advanced rubber compounds. This can lead to the development of innovative solutions and the improvement of existing technologies, giving manufacturers a competitive edge in the market.
During the development of new disposable syringe models, manufacturers use the test chamber to evaluate the performance of prototypes under various temperature and humidity conditions. This includes testing the physical properties of the syringe components, such as the strength and flexibility of the plastic, as well as the functionality of the syringe, such as the ease of filling and injection. The test results are used to make design improvements and ensure that the final product meets the desired performance and quality standards.
In the manufacturing process, the test chamber is used for quality control purposes. A sample of disposable syringes from each production batch is tested in the chamber to ensure that they meet the specified quality standards. The precise control of temperature and humidity allows for accurate evaluation of the syringes' performance, and any issues can be identified and addressed before the products are shipped to the market.
To determine the shelf - life of disposable syringes, manufacturers conduct shelf - life testing in the test chamber. This involves subjecting the syringes to extended periods of controlled temperature and humidity conditions to simulate the effects of long - term storage. The data collected during these tests helps in predicting the syringe's lifespan and determining the appropriate storage conditions to maintain its quality and functionality.
The test chamber can be used to conduct compatibility testing of disposable syringes with different medications and solutions. By exposing the syringes to various temperature and humidity conditions while in contact with different substances, manufacturers can evaluate the potential for chemical reactions or degradation. This helps in ensuring that the syringes are safe and compatible with a wide range of medications, reducing the risk of adverse effects for patients.
Our high - precision medical temperature humidity test chamber for disposable syringes is an essential tool for the medical device industry. With its ultra - high precision control, customizable test profiles, high - volume capacity, advanced monitoring and data logging, material compatibility and hygiene, and safety features, it provides a comprehensive and reliable platform for testing, evaluating, and improving disposable syringes. Whether it's for new syringe development, quality control, shelf - life testing, or compatibility testing, this test chamber is crucial for ensuring the safety, quality, and reliability of disposable syringes in the global healthcare market. Contact us today to learn more about how our product can meet your specific testing needs.
