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Pharmaceutical Stability Test Chamber

Pharmaceutical Stability Test Chamber

Product Introduction
Pharmaceutical stability test chamber is used for research in the pharmaceutical industry, medicine, biotechnology industry and all related industries including life sciences. GMP principles require 25℃/60%RH humidity long-term stability test conditions. In the accelerated test 40 ℃ / 75% RH humidity test 6 months standard, is the pharmaceutical industry stability test requirements. Pharmaceutical stability test chamber mainly simulates the environmental climate in the temperature, humidity, light test.

Service Hotline

4000-662-888
Product Features
Product Parameter
Model Studio Size  (D*W*H)mm Dimension(D*W*H)mm
YP-150SD 500×500×600 1220×770×1730
YP-250SD 680×500×730 1400×770×1860
YP-500SD 700×800×900 1210×1000×1900
YP-010SD 1000×1000×1000 1200×1500×2200
temperature range 0℃~65℃
Humidity range 40%~95%RH
Constant temperature fluctuation temperature ±0.5℃
Constant temperature fluctuation humidity ±3%RH
Time Setting Range 1~9999H
Outer case material High quality A3 steel plate electrostatic spraying
Inner box material Imported high-grade stainless steel SUS304
Insulation material Rigid polyurethane foam + fiberglass
Temperature and humidity controller Korea TEMI330
Temperature and humidity sensors PT100 platinum resistance temperature measurement body
Cooling method stand-alone refrigeration
Compressor Taikang, France
standard configuration 1 roll of wet bulb gauze, 1 water pump, 1 water tank, 2 sample shelves
security protection Compressor overpressure overload, over-temperature, fan motor overheating, the whole machine under phase / reverse phase
Overall equipment timing, leakage protection, overload and short-circuit protection, water shortage protection
Supply Voltage AC220V±10% 50±0.5Hz AC380V±10% 50±0.5Hz
Power 4.0kW/6.0kW/9.0kW/11kW
operating environment 5℃~+28℃ ≤85% RH
Note:
1、the above data are in the use of ambient temperature of 25 ℃ and well ventilated conditions measured
2、Can be customized according to the specific requirements of the user non-standard pharmaceutical stability test chamber etc
3、This technical information, subject to change without notice

 

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