Product Overview
The drug stability test chamber is manufactured in accordance with the "GB10586-2006 Technical Conditions for Wet Heat Chambers". It is suitable for stability tests of pharmaceutical companies' drugs and new drugs, and meets the technical conditions of accelerated tests, long-term tests, and high and low temperature wet heat tests specified in the GMP, FDA, and ICH principles.
Main Features
1. The box body is made of high-pressure polyurethane, with excellent thermal insulation performance and is sturdy and reliable.
2. The exterior of the box body is sprayed with high-quality cold-rolled steel plates, and the interior is made of brushed stainless steel liner. The shelf spacing in the box is adjustable.
3. It uses a brand compressor and environmentally friendly fluorine-free refrigerant (R134a), which is high-efficiency, low-energy consumption, energy-saving and environmentally friendly.
4. Microcomputer PID control, precise and reliable temperature control, less fluctuation, with timing function.
5. SMOOTH overall air duct uniform system, more accurate temperature control.
6. Independent temperature limit alarm system, dual temperature limit (±4℃ and upper limit 70℃) protection, automatic interruption when exceeding the limit temperature.
7. Contains built-in printer and USB data memory storage acquisition function to record temperature change parameters.
8. LCD display, clock display and timing function are convenient for observing the cultivation time, and the timing time can be set from 0 to 9999 minutes.
9. There is a test hole with a diameter of 30mm on the left side of the box, which is convenient for experimental operation and temperature measurement.
10. Self-diagnosis function, automatic monitoring of faults throughout the process, and intuitive indication of fault codes.
11. Using balanced control mode, the humidifier uses a large water tank with a built-in humidifier ring system, which can effectively reduce the frequency of water addition (add water once every 10-15 days), and the humidity control accuracy is more accurate
12. The illumination is adjustable.
13. Implementation and compliance standards: 2020 edition of the Pharmacopoeia Drug Stability Test Guidelines (GMP) and GB/T10586-2006 related provisions.
14. Inner box dimensions: 1080×490×1000mm
15. External dimensions: 1150×650×1620mm
16. Carrier bracket (standard): 6