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Mini-Environment Cleanroom

Mini-Environment Cleanroom

Mini-Environment Cleanroom

Custom high-precision constant temperature and humidity clean micro-environments are engineered for sterile biopharmaceutical workflows, semiconductor packaging processes and advanced laboratory R&D. Cleanliness ratings extend up to ISO Class 2, with configurable ISO Class 5 (Class 100) and ISO Class 6 (Class 1000) options. Biopharmaceutical variants fully align with FDA cGMP requirements under 21 CFR Part 210 and 211. Semiconductor and electronics models follow ISO 14644 and SEMI specifications to rigorously control particulate contamination and airborne molecular contaminants (AMCs).

Precision Control Capabilities

Precision Control Capabilities

Temperature uniformity and stability: ±0.1℃ Ultra-precise closed-loop temperature regulation suppresses thermal fluctuations, meeting the stringent thermal tolerance standards for wafer inspection and sensitive biological specimen testing.
Relative humidity stability: ±2% RH Constant humidity control eliminates static charge accumulation and prevents moisture-induced material degradation. It stops electrostatic adsorption of particulates to sustain consistent cleanroom cleanliness at all times.
Maximum cleanliness level: ISO Class 2 ULPA filtration systems deliver ultra-high particulate removal efficiency. Switchable laminar and turbulent airflow modes are provided to balance performance: laminar flow serves vibration-sensitive electronics manufacturing, while turbulent airflow caters to sterile biotech production sequences.
Optional anti-vibration base system and customized structural configurations An optional integrated anti-vibration base platform is available. Overall footprint, internal layout and structural frames can be fully personalized to seamlessly integrate with semiconductor precision metrology equipment and biopharmaceutical testing workstations.