Friability Test Apparatus

Labpro 255 Tablet Friability Apparatus is a precision laboratory instrument designed to evaluate the mechanical strength and durability of pharmaceutical tablets. Built with robust materials and accurate rotation control, it ensures consistent and reliable friability testing in compliance with pharmacopeial standards. The apparatus is widely used in quality control laboratories, research facilities, and pharmaceutical manufacturing units for routine tablet testing. This friability tester features a transparent drum for easy observation, smooth operation, and user-friendly controls for efficient testing. Its compact design, stable performance, and low maintenance make it ideal for daily laboratory use. The Labpro 255 Tablet Friability Apparatus helps manufacturers maintain tablet quality, reduce breakage issues, and ensure safe, effective pharmaceutical products.

The HTLP-073 Friability Test Apparatus is a laboratory instrument used to assess the friability of tablets, which is their tendency to break or crumble when subjected to mechanical stress. This apparatus helps pharmaceutical companies ensure the quality and integrity of their tablet formulations by simulating the conditions tablets may encounter during handling and transportation. Key features of the HTLP-073 Friability Test Apparatus include: Voltage Compatibility: The apparatus operates on a voltage of 220-230V AC, making it compatible with standard electrical outlets commonly found in laboratory settings. Rotating Drum: The core component of the apparatus is a rotating drum or cylinder where the tablets are placed for testing. The drum rotates at a controlled speed to subject the tablets to tumbling and abrasion, simulating the mechanical stresses encountered during transportation and handling. Precise Control: The apparatus offers precise control over the rotation speed and duration of the test, allowing users to tailor the testing conditions to specific requirements or regulatory standards. Sample Capacity: Depending on the model, the apparatus may have a variable sample capacity, accommodating multiple tablets for simultaneous testing. This feature improves testing efficiency and throughput, especially in high-volume production environments. Durable Construction: Constructed from high-quality materials, the apparatus is durable and built to withstand the rigors of laboratory use. Its robust design ensures long-term reliability and consistent performance. Easy Operation: The HTLP-073 Friability Test Apparatus is designed for ease of use, with intuitive controls and a user-friendly interface. Operators can quickly set up and initiate tests without extensive training. Accurate Results: By subjecting tablets to controlled mechanical stress, the apparatus provides valuable insights into the friability characteristics of tablet formulations. Accurate and reproducible test results help pharmaceutical companies assess product quality and make informed decisions regarding formulation and manufacturing processes. Compliance with Standards: The apparatus may comply with relevant industry standards and regulations governing tablet friability testing, ensuring adherence to best practices and quality assurance protocols. In summary, the HTLP-073 Friability Test Apparatus is a valuable tool for pharmaceutical companies seeking to evaluate the friability of their tablet formulations. With its precise control, sample capacity, and durable construction, this apparatus offers reliability, efficiency, and accuracy in tablet quality assessment.

A Labpro 70 Digital Friability Apparatus, also known as a friability tester or friabilimeter, is a device used to determine the friability or resistance to abrasion of tablets or granules. The friability test is an important quality control test performed in the pharmaceutical industry to assess the durability and stability of oral solid dosage forms. The main purpose of the friability test is to evaluate the tendency of tablets or granules to undergo physical degradation or erosion during handling, transportation, and packaging. The test helps to determine the potential for the tablets to crumble or break apart, which can affect their effectiveness and dosing accuracy. The basic components of a friability test apparatus include: Drum: The test samples, typically a specified number of tablets or granules, are placed inside a rotating drum. The drum is made of a transparent material, usually glass or plastic, to allow observation of the samples during the test. Rotation Mechanism: The drum is rotated at a fixed speed, typically between 25 and 100 revolutions per minute (RPM), for a specific duration. The rotation causes the tablets or granules to collide with each other and the drum wall, simulating the mechanical stress they may encounter during handling. Timer: A timer is used to control the duration of the test. The test duration is typically set at 4 minutes, although variations may exist depending on the specific test method or pharmacopoeial requirements. Sample Collection Tray: After the test is completed, the drum is stopped, and the samples are collected from the drum. Any fragmented or eroded particles that have been generated during the test are separated from the intact tablets or granules. Balance: A balance or weighing scale is used to measure the weight loss of the samples. The weight loss is an indication of the friability or propensity of the tablets or granules to lose mass during the test. The friability test is performed by subjecting the test samples to a specified number of rotations in the apparatus. After the test, the samples are re-weighed to determine the percentage weight loss. The weight loss is calculated as a percentage of the initial sample weight, and the results are compared against the acceptance criteria specified in pharmacopoeial standards or internal quality control guidelines. The friability test apparatus provides valuable information about the mechanical strength and integrity of tablets or granules. It helps pharmaceutical manufacturers ensure that their products can withstand normal handling and transportation conditions without excessive damage or degradation. By performing the friability test, potential issues related to tablet formulation, compression, or coating processes can be identified and addressed. It's important to note that different pharmacopoeias or regulatory bodies may have specific guidelines and requirements for the friability test method and acceptance criteria. Manufacturers should adhere to the relevant standards and procedures to ensure compliance with regulatory requirements and maintain the quality and consistency of their pharmaceutical products.

Technical Specifications :-
Transparent Plastic Drum
Rotating Plastic Drum For Rots
Plastic Blades
Where Tablet Friability Test Apparatus Used?
Institutes
Medical Colleges
Industries
Pharmacy Colleges
Pharmaceutical Industry
Laboratories
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The HTLP-073 Friability Test Apparatus with Digital RPM Counter is a specialized laboratory instrument used to evaluate the friability of tablets, assessing their propensity to break or crumble under mechanical stress. This apparatus offers precise control and accurate measurement of rotational speed through its digital RPM counter, enhancing the reliability and reproducibility of test results. Key features of the HTLP-073 Friability Test Apparatus with Digital RPM Counter include: Digital RPM Counter: The apparatus is equipped with a digital RPM (Rotations Per Minute) counter, which accurately measures the rotational speed of the drum or cylinder where the tablets are placed. This feature provides precise control over the testing parameters, ensuring consistency and repeatability in test conditions. Rotating Drum: Tablets under evaluation are placed inside a rotating drum or cylinder, which simulates the mechanical stresses encountered during handling and transportation. The digital RPM counter allows users to monitor and adjust the rotational speed of the drum according to test requirements. Variable Speed Control: The digital RPM counter enables users to adjust the rotational speed of the drum to suit specific testing protocols or regulatory standards. This variable speed control feature allows for flexibility in testing conditions and facilitates accurate characterization of tablet friability. Sample Capacity: Depending on the model, the apparatus may accommodate a variable number of tablets for testing, allowing for simultaneous evaluation of multiple samples. This enhances testing efficiency and throughput, especially in high-volume production environments. Durable Construction: Constructed from high-quality materials, the apparatus is durable and designed to withstand the rigors of laboratory use. Its robust construction ensures long-term reliability and consistent performance in friability testing applications. Easy Operation: The HTLP-073 Friability Test Apparatus with Digital RPM Counter is user-friendly, featuring intuitive controls and a clear digital display for monitoring test parameters. Operators can easily set up tests, initiate measurements, and interpret results with minimal training. Accurate Measurement: The digital RPM counter provides accurate measurement of rotational speed, allowing for precise control and documentation of test conditions. This accuracy enhances the reliability and validity of test results, supporting informed decision-making in tablet formulation and manufacturing processes. Compliance with Standards: The apparatus may comply with relevant industry standards and regulations governing tablet friability testing, ensuring adherence to best practices and quality assurance protocols. In summary, the HTLP-073 Friability Test Apparatus with Digital RPM Counter offers advanced features for precise and reliable evaluation of tablet friability. With its digital RPM counter, variable speed control, and durable construction, this apparatus provides pharmaceutical companies with a valuable tool for assessing tablet quality and optimizing manufacturing processes.

A Labpro 243 Sterility Three Test with Stainless Steel Flask Clamps, also known as a friability tester or friabilimeter, is a device used to determine the friability or resistance to abrasion of tablets or granules. The friability test is an important quality control test performed in the pharmaceutical industry to assess the durability and stability of oral solid dosage forms. The main purpose of the friability test is to evaluate the tendency of tablets or granules to undergo physical degradation or erosion during handling, transportation, and packaging. The test helps to determine the potential for the tablets to crumble or break apart, which can affect their effectiveness and dosing accuracy. The basic components of a friability test apparatus include: Drum: The test samples, typically a specified number of tablets or granules, are placed inside a rotating drum. The drum is made of a transparent material, usually glass or plastic, to allow observation of the samples during the test. Rotation Mechanism: The drum is rotated at a fixed speed, typically between 25 and 100 revolutions per minute (RPM), for a specific duration. The rotation causes the tablets or granules to collide with each other and the drum wall, simulating the mechanical stress they may encounter during handling. Timer: A timer is used to control the duration of the test. The test duration is typically set at 4 minutes, although variations may exist depending on the specific test method or pharmacopoeial requirements. Sample Collection Tray: After the test is completed, the drum is stopped, and the samples are collected from the drum. Any fragmented or eroded particles that have been generated during the test are separated from the intact tablets or granules. Balance: A balance or weighing scale is used to measure the weight loss of the samples. The weight loss is an indication of the friability or propensity of the tablets or granules to lose mass during the test. The friability test is performed by subjecting the test samples to a specified number of rotations in the apparatus. After the test, the samples are re-weighed to determine the percentage weight loss. The weight loss is calculated as a percentage of the initial sample weight, and the results are compared against the acceptance criteria specified in pharmacopoeial standards or internal quality control guidelines. The friability test apparatus provides valuable information about the mechanical strength and integrity of tablets or granules. It helps pharmaceutical manufacturers ensure that their products can withstand normal handling and transportation conditions without excessive damage or degradation. By performing the friability test, potential issues related to tablet formulation, compression, or coating processes can be identified and addressed. It's important to note that different pharmacopoeias or regulatory bodies may have specific guidelines and requirements for the friability test method and acceptance criteria. Manufacturers should adhere to the relevant standards and procedures to ensure compliance with regulatory requirements and maintain the quality and consistency of their pharmaceutical products.

The LABIX Microprocessor Friability Apparatus, LBX-620, is engineered to deliver precise tablet friability testing with high reliability and ease of use. Equipped with dual drums rotating at a controlled speed of 20 to 60 RPM ±0.5 RPM, this apparatus supports both time and count test modes to accommodate various testing protocols. Its clear 20×4 alphanumeric LCD display paired with soft touch membrane keys ensures intuitive operation and accurate data input. This robust friability tester features a direct drive stepper motor for smooth and consistent rotation, along with a versatile counter capable of counting up to 9999 rotations. The built-in timer ranges from 1 second to nearly 10 hours, while USB connectivity and a parallel printer interface simplify data management and documentation. Compact and durable, the LBX-620 stores up to 200 sample readings with batch and sample numbers, making it ideal for pharmaceutical quality control labs demanding precision and efficiency.

The Labtronics Microprocessor Friability Apparatus, model LT-710, is an advanced instrument designed for assessing the friability of tablets in pharmaceutical quality control. Friability is a critical parameter that measures the tendency of tablets to break or crumble during handling and transportation, providing insight into the tablet's structural integrity and durability.
1. Friability Testing: Friability testing involves subjecting a sample of tablets to mechanical stress, simulating the conditions they might encounter during handling and transportation. The LT-710 measures the weight loss of the tablets due to abrasion and breakage, providing valuable information about the tablet's resistance to physical stress.
2. Microprocessor Control: The integration of a microprocessor in the LT-710 ensures precise control over the friability testing process. This technology allows for accurate speed control, rotation direction, and customizable testing parameters, contributing to the repeatability and reliability of the test results.
3. Double Drums: One distinctive feature of the LT-710 is its double drum configuration. This design allows for simultaneous testing of two samples, increasing the efficiency of the testing process. Testing multiple samples concurrently is particularly beneficial in pharmaceutical laboratories where a high throughput of quality control tests is essential.
4. Applications: The LT-710 is specifically designed for use in pharmaceutical quality control laboratories. Friability testing is a mandatory evaluation according to pharmacopeial standards (e.g., USP - United States Pharmacopeia), ensuring that tablets maintain their structural integrity under normal handling conditions.
5. User-Friendly Interface: The instrument likely features a user-friendly interface, facilitating easy operation, parameter adjustments, and data retrieval. This is crucial for laboratory technicians who need to perform friability tests routinely.
6. Compliance with Standards: The LT-710 is likely designed to comply with industry standards and pharmacopeial requirements for friability testing. This ensures that the apparatus and the testing process adhere to recognized quality control standards.
In summary, the Labtronics Microprocessor Friability Apparatus (LT-710) is an advanced and efficient tool for pharmaceutical quality control, specifically designed for friability testing of tablets. Its microprocessor control, double drum configuration, and compliance with industry standards make it a valuable instrument for ensuring the quality and durability of pharmaceutical tablets.

The Labtronics Digital Friability Test Apparatus is a precision instrument designed to evaluate the friability and durability of tablets during handling and transportation. Compliant with USP and IP standards, it features a microprocessor-controlled digital display that allows programmable settings for both time and revolutions (0 to 9999), ensuring flexible and highly accurate testing. The rotating drum, made of transparent acrylic, allows clear visibility of the tablets during rotation and is driven by a maintenance-free motor that ensures consistent performance. Engineered for pharmaceutical quality control, the apparatus supports both single and dual drum configurations and includes an automatic stop function once the set revolutions or time is reached. The unit is housed in a durable, chemical-resistant body and features a user-friendly interface with soft-touch membrane keys for easy operation. The Labtronics Friability Tester is ideal for R&D and QC labs seeking reliable, repeatable results in tablet durability assessments.

LABCARE LABCARE LB-937 230 V Friability Test Apparatus Single Drum has a single drum. The item can be used in laboratories, schools and factories. The apparatus is made with cast iron body and aluminum alloy. It measures the resistance that tablets have to being crushed into powder using an electric motor, heating element, and torsion spring. It contains a single drum that rotates at a high speed; once a tablet is placed inside the drum, its friability (i.e., its tendency to crumble) can be measured based on the time it takes for the tablet to leave a defined area of the drum. The equipment has three compartments, one each to hold the sample, the working medium (i.e. the mortar) and the pestle. The working medium is like a liquid that grinds the sample into finer particles. The LB-937 230 V Friability Test Apparatus Single Drum is an electrical equipment and will work on single phase voltage of 230 Volts. The unit has an adjustable drop height (1.5-5.0 cm) and a Teflon beaker that can hold up to 1,000 mL. The LB-937 is ideal for use in public works projects and highway construction sites, in which the quality of aggregate can affect the job's longevity and strength. It can be used for the purpose of testing friability by means of screening, classifying and sub-classifying. The apparatus operates on 230 V and has a tumbling speed of 200 rpm. The drum diameter is 500mm and it can be moved in any direction using the spoon feeder system.

The LABCARE LB-938 50Hz 99.59min Range Digital Friability Test Apparatus double drum has features which make the friability test easier and more efficient. It is best suited for the friability test of plastic, rubber and adhesive materials. The machine is designed to be used in laboratory conditions only. The capacity of the machine is up to 130 tests per hour. The LB-938 has a digital display screen and can store data in a USB drive or external memory device. . The two separate drums in the LB-938 are completely independent and all the parameters can be set individually. The device uses 50Hz frequency (60Hz version available) and the time can be set from 99.59 minutes to 99.99 hours. The LB-938 has a digital display for timer function, which can be clearly read by users. The LB-938 comes with an automatic data output function and its powerful software will calculate all results automatically without manual operation. It is a double drum tester, which means that it uses dual drums rotating at the same time to test your material. This setup can cut your testing time in half, and helps ensure that the results are consistent from one test to another. It also allows for more accurate readings on the initial sample size than a single drum tester would be able to achieve.

The NSAW Friability Test Apparatus NSAW-1665 is a specialized instrument used in pharmaceutical quality control laboratories to assess the friability of tablets. Friability testing is an essential step in the evaluation of solid dosage forms, ensuring that tablets maintain their integrity and do not excessively crumble or break during handling and transport. The NSAW-1665 apparatus typically consists of a drum or rotating chamber where a sample of tablets is placed. The drum rotates at a specified speed for a predetermined duration, causing the tablets to collide with each other and the chamber walls. After the test cycle, the tablets are removed, and the amount of friability is determined by measuring the weight loss or the percentage of tablet mass lost due to abrasion and breakage. The NSAW Friability Test Apparatus NSAW-1665 is equipped with precision timing mechanisms and speed controls to ensure consistent test conditions. It may also include features such as adjustable drum rotation speeds, automated sample handling, and digital displays for easy monitoring of test parameters. Friability testing helps pharmaceutical manufacturers assess the robustness of their tablet formulations and evaluate the impact of manufacturing processes on tablet integrity. It is an important quality control measure to ensure that tablets remain intact and deliver the correct dose of medication to patients throughout their shelf life.

Lab Junction Single Wheel Digital Friability Test Apparatus LJ-903 is a specialized device used in the pharmaceutical industry to assess the physical strength and durability of tablets or granules. It measures the tendency of these solid dosage forms to undergo erosion or breakage during handling, packaging, and transportation. The test is important for ensuring the quality, stability, and performance of oral medications.
The digital friability test apparatus consists of a rotating drum or a rotating paddle that holds the sample tablets or granules. The drum or paddle rotates at a specified speed for a predetermined period, subjecting the samples to mechanical stress. After the test cycle is completed, the apparatus measures the amount of weight loss or damage experienced by the tablets or granules.
The digital aspect of the apparatus refers to its electronic monitoring and control features. It typically includes a digital display screen that shows the test parameters and results, as well as buttons or touch controls for adjusting settings. This allows for accurate and precise control of the test conditions, such as rotation speed and test duration.
During the friability test, the tablets or granules are subjected to repeated impacts and collisions within the rotating drum or against the rotating paddle. This simulates the physical stresses that the dosage form may encounter during handling and transport. The extent of weight loss or damage is an indication of the tablet's ability to withstand such stress without excessive erosion or breakage.
The digital friability test apparatus provides several benefits over manual or older mechanical versions. It offers improved accuracy, repeatability, and reproducibility of test results. The digital display allows for easy reading and recording of data, minimizing errors and enhancing data integrity. The electronic control features enable precise control of test parameters, ensuring consistent testing conditions across multiple samples and test runs.
The results obtained from the digital friability test can be used for quality control purposes in the pharmaceutical industry. They help determine the physical robustness and resistance to erosion of tablets or granules, ensuring that they meet the required standards and can withstand handling and transportation without significant degradation. Deviations from the acceptable friability limits may indicate the need for process adjustments or formulation improvements.
In summary, a digital friability test apparatus is a specialized device used to evaluate the physical strength and durability of tablets or granules in the pharmaceutical industry. It utilizes a rotating drum or paddle to subject the samples to mechanical stress and measures the weight loss or damage experienced. The digital features provide accurate control, monitoring, and recording of test parameters and results. The test results help ensure the quality and stability of oral medications by assessing their resistance to erosion and breakage during handling and transportation.

Used For Tablets To Determine The Durability At The Time Of Production. A Transparent Plastic Perspex Drum With Cover Also A Shaped Radial Fixed Blade Which Carries The Tablets Along with It Upto The Central Height And Lets Them Off While The Drum Is Rotating, Thus The Tablet Rub Against Each Other Without Any Hard Impact. The Drum Rotates At A Fix Speed Of 30 Rpm By A Geared Motor. The Rotation Period Is Determined By A Electric Timer. Tablets Are Weighed Before And After The Test And The Difference In Weight For A Particular Time Period Indicating The Rate Of Abrasion. Complete With Electric Timer With Neon Indicators Fitted On A Panel.

The Vesca VSLI-279 Friability Test Apparatus With Digital RPM Counter Made of Acrylic Sheet is a precision laboratory instrument designed to evaluate the mechanical strength and durability of pharmaceutical tablets. Featuring a durable acrylic sheet construction, the Vesca VSLI-279 Friability Test Apparatus With Digital RPM Counter Made of Acrylic Sheet provides clear visibility of tablets during testing, ensuring accurate observation of weight loss and surface wear. The integrated digital RPM counter allows precise monitoring and control of rotational speed, enhancing the reproducibility and accuracy of friability assessments. The Vesca VSLI-279 Friability Test Apparatus With Digital RPM Counter Made of Acrylic Sheet combines user-friendly operation, reliable performance, and robust design, making it an essential tool for pharmaceutical laboratories engaged in quality control, formulation analysis, and routine tablet testing. Engineered for consistency and efficiency, the Vesca VSLI-279 Friability Test Apparatus With Digital RPM Counter Made of Acrylic Sheet ensures uniform rotation and controlled impact, simulating real-world handling conditions that tablets encounter during packaging and transport. The digital RPM counter provides precise feedback on speed, allowing researchers to maintain standardized testing conditions across multiple samples. The Vesca VSLI-279 Friability Test Apparatus With Digital RPM Counter Made of Acrylic Sheet is ideal for laboratories focused on quality assurance, formulation optimization, and regulatory compliance. Its combination of transparent acrylic construction, digital monitoring, and reliable performance ensures accurate, reproducible, and high-quality friability test results for pharmaceutical tablets.

The Vesca VSLI-279 Friability Test Apparatus Made of Acrylic Sheet and 220/230 V AC Working Voltage is a laboratory instrument designed to assess the mechanical strength and durability of pharmaceutical tablets. Constructed with a robust acrylic sheet, the Vesca VSLI-279 Friability Test Apparatus Made of Acrylic Sheet and 220/230 V AC Working Voltage ensures transparency for easy observation of tablet behavior during testing while providing durability and resistance to wear. Operable on a standard 220/230 V AC power supply, this apparatus delivers consistent rotational motion to evaluate tablet friability accurately, helping laboratories maintain quality control and compliance with pharmaceutical standards. The Vesca VSLI-279 Friability Test Apparatus Made of Acrylic Sheet and 220/230 V AC Working Voltage combines precision, reliability, and user-friendly operation, making it an essential tool for research, formulation analysis, and routine quality assessments in pharmaceutical settings. Engineered for accuracy and efficiency, the Vesca VSLI-279 Friability Test Apparatus Made of Acrylic Sheet and 220/230 V AC Working Voltage provides controlled rotation and uniform impact to simulate handling conditions that tablets may experience during packaging and transportation. Its acrylic construction allows clear visibility of tablets throughout the test, ensuring accurate observation and measurement of weight loss or surface damage. The Vesca VSLI-279 Friability Test Apparatus Made of Acrylic Sheet and 220/230 V AC Working Voltage is ideal for pharmaceutical laboratories focused on quality assurance and formulation development. With durable construction, precise performance, and easy operation, the Vesca VSLI-279 Friability Test Apparatus Made of Acrylic Sheet and 220/230 V AC Working Voltage guarantees reproducible and reliable results for tablet friability evaluation.

Electronic India Digital Friability Test Apparatus
Key Features :
Sturdy motor to drive drums at constant speed
Seven segment LED display
Single Drum Drive
Please Note: Image displayed on the website is a reference , the product specifications will be same however the actual product colour might differ. Kindly check the technical specifications provided in the description to make the better purchase decision.

Digital Friability Test Apparatus is a precision instrument suitable for measuring obression strength of tablets. The unit is equipped with two transparent acrylic drums which rotate at a
Sturdy motor to drive drums at constant speed.
Feature :
This is available in 1 drum assemblies.
speed of 25 ± 1 rpm.
Seven segment LED display

Salient Features:
Fully USP and EP compliant design. Single Drum with quick-change front-load system. Speed and Cyclomatic number of the Drum can be Preset. Preset or Real Data is displayed on the LED. Buzzer Alarm at the completion of the Test. 10 degree tilting function according to USP. Transparent Plastic Perspex Drum Dia 300 x 35 mm deep with cover. Inbuilt Auto-Alarm and indication. Calculation of friability or percentage weight loss can be done manually. Standard Accessories Standard Jaw Plate, Safety Shield, Brush and Tablet Collection Tray Optional Accessories Abrasion Drum