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.
