About Disintegration Test Apparatus Tablet
Empowered by our rich industry experience, we are engaged in providing our clients a broad assortment of Disintegration Test Apparatus Tablet. The offered apparatus is manufactured using the finest grade raw material in compliance with the set industry standards. This apparatus is available in various specifications as per the specific needs of our clients. Widely demanded in the pharmaceuticals industry, institution and research laboratories for disintegration testing of tablets and capsules, this Disintegration Test Apparatus Tablet is available at market leading price.
Efficient Tablet Disintegration TestingThis apparatus provides accurate, repeatable analysis essential for pharmaceutical tablet quality assurance. By precisely monitoring the breakdown of tablets under controlled conditions, it helps labs maintain regulatory compliance and enhance formulation evaluation.
Durable Design for Laboratory UseManufactured from stainless steel, the device offers long-lasting durability and resistance to laboratory environments. Its compact rectangular shape and user-friendly manual scale make it suitable for diverse quality control workflows.
Analog Display with Manual ControlEquipped with a manual analog display, the apparatus ensures users can easily observe and record disintegration results without complex digital interfaces, reducing training time and simplifying operation.
FAQs of Disintegration Test Apparatus Tablet :
Q: How does the Disintegration Test Apparatus function in a laboratory setup?
A: The apparatus immerses tablets in a temperature-controlled liquid, simulating digestive conditions. The manual analog display allows precise monitoring of the disintegration process, ensuring reliable quality control data.
Q: What are the main benefits of using this apparatus for tablet quality control?
A: This device provides high-precision and consistent results, is durable thanks to its stainless steel construction, and offers straightforward manual operation, making it ideal for routine pharma testing environments.
Q: When should pharmaceutical manufacturers use this apparatus?
A: It should be used during the quality control stage of tablet development and prior to batch release, ensuring each tablet batch meets regulatory standards for disintegration.
Q: Where is this apparatus commonly utilized?
A: This test apparatus is widely used in pharmaceutical laboratories, research centers, and manufacturing quality control departments across India.
Q: What is the typical process for performing a disintegration test with this device?
A: Tablets are placed in the apparatus baskets, which are then immersed in a liquid at ambient to 37C. The apparatus is activated, and the operator times and records how long it takes for each tablet to completely disintegrate.
Q: What makes this apparatus suitable for laboratory use in terms of accuracy and durability?
A: It features high-precision measurement, a standard height for compatibility, stainless steel build for longevity, and durable construction to withstand daily lab operations.