Comprehensive medicine Stability test chamber FS/CFS

Labonce-FS Medicine Stability Testing Chamber,Adopt imported process design,Choose the original imported high quality parts, Stable and reliable performance,Equipped with imported full electronic recording system,With audit tracking function,Comply with the FDA 21 CFR PART Ⅱ law standard,With 8 language interface to fully meet the needs of different users facing the global customers,Suitable for CGMP certified users.

1.The newly airway system designed achieves uniform of temperature and humidity form different parts inside the chamber; Polyurethane foam technology is adopted, with good heat preservation and moisture retention performance.

2. The original imported VAISALA humidity sensor with high accuracy, low drift, long life and maintenance free.

3.The original imported fully enclosed industrial compressor, high efficiency, low noise, ensure the long-term continuous operation of equipment.

4. The original imported programmable chromatic touch screen controller, sensitive, Small system error, Multi - stage program setting and multi - point accurate calibration function, With three level password.

5. There is a 25mm diameter test hole on the left side of the box. The stability chambers with capacity of 800L or above is designed with double doors. The inside toughened glass door and the outside door are designed to observe samples and It will not cause the change of temperature and humidity in the box in a short time.Door lock and mobile caster can be locked.

6. The liner is made of mirror stainless steel 304, no pollution source, easy to clean.

7. Date system: Needle micro printer,SD card storage and online electronic recording.

8.Safety device: Compressor overheat and over pressure overload protection, water shortage protection, dry burning protection system, independent over temperature protection alarm system;

9. Alarm system: Sound-light alarm for temperature and humidity deviation, SMS alarm for remote temperature and humidity deviation and power failure, email alarm.

10.Meet ICH2003、Pharmacopoeia 2015 edition，Executive standard：GB/T 10586-2006；

11.Temperature Fluctuation：≤ ±0.5℃，Temperature Deviation：≤ ±1.0℃；Humidity Deviation：≤ ±3%RH

12.Electronic recording system,Comply with the FDA 21 CFR Part Ⅱ law standard,Stable system performance,Audit tracking function,Three levels of user hierarchical authority management.