EI-DVI model 1918 Microprocessor Dissolution Test Apparatus

EI-DVI
SKU:
EI-1918
₹293,820.00 (Including GST)
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EI-DVI Model 1918 Microprocessor Dissolution Test Apparatus – Advanced Pharmaceutical Dissolution Testing System

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.

Technical Specifications

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

Core Features & User Benefits

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.

  • USP & IP Compliant Dissolution Testing Designed to meet internationally accepted pharmaceutical testing standards for reliable dissolution analysis and regulatory compliance.
  • Advanced Microprocessor Control High-performance microprocessor technology ensures precise control of temperature, RPM, and test timing for highly reproducible analytical results.
  • 8 Station Testing System Multiple vessel configuration allows simultaneous testing of multiple pharmaceutical samples, improving laboratory throughput and operational efficiency.
  • Large Backlit LCD Display The 20 x 4 line alphanumeric display provides clear real-time visibility of testing parameters, settings, and operational status.
  • Programmable Test Method Storage Users can store up to 20 different test methods and 200 sample records for efficient workflow management and repeat testing.
  • Precise RPM Control Programmable stirrer speed control from 25 to 200 RPM with ±1 RPM accuracy ensures dependable dissolution testing performance.
  • Dual Temperature Monitoring Simultaneous monitoring of vessel and water bath temperatures improves thermal stability and testing consistency.
  • Motorized Sampling Platform The automated up/down platform movement simplifies manual sampling and improves accessibility during testing procedures.
  • Power Failure Resume Function Intelligent memory backup retains current test status and resumes operation after power restoration, minimizing sample loss and operational disruption.
  • Integrated Printer Connectivity Supports dot matrix printer attachment for convenient printing of test setups, stored methods, and dissolution test results.

Frequently Asked Questions (FAQ)

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.