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Drug Stability Test Chamber NDSTC-100 Data Sheet

Laboratory Equipment
Product Series / Drug Stability Test Chamber
Drug Stability Test Chamber
NDSTC-100
500 L Volume
0 to 70 °C Temperature Range
0.1 °C Temperature Resolution
Drug Stability Test Chamber NDSTC-100
Labnics Product Data Sheet · Laboratory Equipment
Drug Stability Test Chamber

Drug Stability Test Chamber NDSTC-100

Drug Stability Test Chamber NDSTC-100 offers a volume of 500 liters and operates within a temperature range of 0 to 70 °C. It features a multi-parameter LCD controller with a locking function and customizable settings with up to 99 cycle segments. Our system includes audible and visual alarms for monitoring condenser blockages and cleaning alerts. It utilizes annular airflow and forced convection for stable chamber conditions. Equipped with a high-quality compressor for continuous operation without failures, increasing drug testing reliability.

Key metrics
500 L
Volume
0 to 70 °C
Temperature Range
0.1 °C
Temperature Resolution
Drug Stability Test Chamber NDSTC-100
Labnics Ltd.

Specifications

Volume 500 L
Temperature Range 0 to 70 °C
Temperature Resolution 0.1 °C
Temperature Uniformity ≤ 0.5 °C
Temperature Fluctuation ± 0.5 °C
Operating Ambient Temperature 5 to 30 °C
Humidity Control Range 30% to 95% RH
Humidity Fluctuation ± 3% RH
Continuous Working Time No less than 9999 h
Load Tray 3 pieces
Power Consumption 2000 W
Dimensions 900 × 850 × 1910 mm
Chamber Dimensions 600 × 730 × 1200 mm
Weight 280 kg
Drug Stability Test Chamber NDSTC-100 · Product Details

Optional Accessories

Optional RS 485 interface

Standard Accessories

Printer
UV disinfection lamp
Test hole: a 45mm diameter test hole produced by a special abrasive tool is set on the side of the box to facilitate user inspection. (Optional)

Features

  • Stainless steel chamber
  • Low energy consumption
  • Fluorine-free design
  • Honeywell humidity sensor
  • High-performance humidifier
  • Compliance with FDA and ICH standards

Applications

Drug Stability Test Chamber is used in the pharmaceutical industry for drug stability inspection and testing. They are essential for determining the validity period of medications and identifying the factors that influence drug stability.
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