EI-DVI Model 2914 Microprocessor Tablet Dissolution Test Apparatus
EI-DVI
The EI-DVI Model 1918 Microprocessor Dissolution Test Apparatus is a highly advanced and precision-engineered pharmaceutical laboratory instrument designed for accurate dissolution testing of tablets, capsules, and other solid dosage formulations. Developed for pharmaceutical quality control laboratories, research and development facilities, formulation development centers, and academic institutions, this dissolution testing apparatus complies with both USP and IP specifications, ensuring dependable and standardized analytical performance.
Powered by modern microprocessor technology and advanced electronic control systems, the EI-DVI Model 1918 provides highly accurate control of dissolution parameters including temperature, stirrer speed, and test duration. The instrument features an intuitive user interface with a large backlit 20 x 4 alphanumeric LCD display and soft touch membrane keypad, enabling easy setup, operation, and monitoring of dissolution testing procedures.
The apparatus supports programmable testing functionality with multiple operational modes including Routine, Sustain, and Control modes. Users can store up to 20 independent test methods and maintain records for up to 200 samples, significantly improving laboratory productivity and data management efficiency.
The sturdy acrylic water bath incorporates a large stainless-steel heater to ensure uniform temperature distribution across all dissolution vessels. Dual channel temperature monitoring continuously supervises both vessel temperature and water bath conditions, enhancing analytical accuracy and reproducibility during testing.
Featuring a motorized up/down stirrer platform for convenient manual sampling access, programmable RPM control, power failure memory protection, and printer connectivity support, the EI-DVI Model 1918 Dissolution Test Apparatus delivers an ideal combination of precision, operational flexibility, and pharmaceutical compliance for modern analytical laboratories.
| Parameter / Feature | Details |
|---|---|
| Product Type | Microprocessor Dissolution Test Apparatus |
| Model | EI-DVI Model 1918 |
| Compliance Standards | USP & IP Specifications |
| Number of Stations | 8 Stations |
| Display | 20 x 4 Line Alphanumeric LCD with Backlit |
| Keyboard Type | 19 Soft Touch Membrane Keys |
| Reaction Vessel Capacity | 1000 ml |
| Stirrer Speed Range | 25 – 200 RPM |
| Stirrer Speed Accuracy | ± 1 RPM |
| Speed Resolution | 1 RPM |
| Temperature Range | 30°C – 50°C |
| Temperature Accuracy | ± 0.2°C |
| Temperature Control | Microprocessor Based using PT100 / Semiconductor Sensor |
| Heater Power | 1 KW |
| Programmable Modes | Routine, Sustain, Control |
| Programmable Test Setups | 20 Independent Setups |
| Sample Storage Capacity | 200 Samples |
| Motorized Platform | Up / Down Movement for Easy Sampling |
| Printer Interface | Centronics Parallel Port for Dot Matrix Printer |
| Temperature Monitoring | Dual Channel Monitoring System |
| Water Bath | Acrylic Tank with Bottom Drainage |
| Power Supply | 230 V ±10% AC, 50 Hz |
| Application Areas | Pharmaceutical QC Labs, R&D Laboratories, Dissolution Testing, Drug Release Studies |
The EI-DVI Model 1918 Dissolution Test Apparatus is engineered to deliver superior pharmaceutical dissolution analysis with enhanced operational reliability, precise control, and regulatory compliance.
What is the primary application of the EI-DVI Model 1918 Dissolution Test Apparatus?
The EI-DVI Model 1918 is primarily used for dissolution testing of pharmaceutical tablets, capsules, and solid dosage forms to determine the release characteristics of active drug ingredients.
It is widely used in pharmaceutical quality control laboratories, formulation development centers, research institutions, and regulatory testing laboratories.
Does the EI-DVI Model 1918 comply with pharmaceutical testing standards?
Yes, the instrument is fully designed to comply with both USP (United States Pharmacopeia) and IP (Indian Pharmacopoeia) dissolution testing specifications.
This compliance ensures reliable analytical performance and suitability for regulated pharmaceutical laboratory environments.
What is the RPM control range of the apparatus?
The EI-DVI Model 1918 provides programmable stirrer speed control from 25 RPM to 200 RPM with an accuracy of ±1 RPM.
This precise speed control helps maintain consistent hydrodynamic conditions during pharmaceutical dissolution testing.
How many test methods and samples can be stored in the system?
The apparatus supports storage of up to 20 independent programmable test setups along with automatic storage for up to 200 samples.
This memory capability significantly improves laboratory workflow efficiency and repeat testing convenience.
What safety and operational convenience features are included?
The system includes a motorized up/down platform for easier manual sampling, power failure recovery functionality, dual temperature monitoring, and LED status indicators for operational monitoring.
These features improve testing reliability, reduce operator workload, and enhance laboratory productivity during dissolution analysis procedures.