Product Description

The Labmart Disintegration Rate Test Apparatus KI-2066-B WB V1 is a high-precision pharmaceutical testing instrument designed to accurately determine the disintegration time of tablets, capsules, and other solid dosage forms in accordance with pharmacopeial standards. Developed for pharmaceutical quality control, research laboratories, formulation development, and academic institutions, this advanced apparatus ensures reliable and reproducible testing results for drug quality assessment.

Engineered with a water bath (WB) system, the KI-2066-B WB V1 provides precise temperature control and uniform heating conditions, enabling accurate simulation of physiological environments during disintegration testing. Its robust construction, user-friendly controls, and dependable performance make it an essential instrument for pharmaceutical manufacturers and quality assurance laboratories seeking compliance with USP, IP, BP, and other international testing standards.

Key Features

  • Advanced water bath system for uniform temperature maintenance
  • Accurate tablet and capsule disintegration testing
  • Digital temperature monitoring and control
  • Reliable basket-rack assembly movement for consistent results
  • High-quality stainless steel and corrosion-resistant construction
  • User-friendly operation with easy-to-read controls
  • Designed for continuous laboratory and quality control applications
  • Suitable for pharmaceutical, research, and educational laboratories

Product Specifications:

Model No. KI- 2066-B WB V1
  Stage/ Basket     Double  
  Rotation Speed     30 (+ 1rpm)  
  Timer     99:59 (100 Mins)  
  Temperature     Ambient to 80°C   
  Heater     65 Watt  
  Display     16X2 ?- Numeric LCD  
  Water Bath     Available  
  Beakers     2X 1000ml  
  Drive System     AC Motor  
  Power     220V+10% 50Hz  
  Dimensions     370 x 340 x 530mm  
  Weight     13.100 Kg.  

 

The Labmart Disintegration Rate Test Apparatus helps researchers and manufacturers evaluate the performance, consistency, and effectiveness of oral solid dosage forms, ensuring product quality and regulatory compliance throughout the pharmaceutical production process.

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