Laboratory shoe cabinets are critical components in contamination control strategies for cleanrooms and safety areas. Our specialized solutions serve pharmaceutical manufacturing, biotechnology laboratories, and healthcare institutions.
Standards ComplianceOur shoe cabinets meet ISO 14644 requirements for cleanroom classifications 5-8 and GMP guidelines. Designed in accordance with FDA 21 CFR Part 11 for electronic records and sterile manufacturing environments.
Material ConstructionCabinet bodies are fabricated from AISI 304 or 316L stainless steel with electropolished surfaces achieving Ra ≤ 0.4 μm roughness. All corners feature radius ≥ 50 mm to eliminate cleaning dead zones. TIG welding creates seamless joints.
Contamination Barrier DesignCabinets employ strict zoning separating "dirty" and "clean" areas. Dual-compartment configuration with physical barriers prevents cross-contamination between non-sterile and sterile surfaces.
Ventilation SystemsIntegrated HEPA H14 filtration provides continuous air exchange, maintaining ISO Class 7 conditions internally. Optional UV-C germicidal lamps (254 nm) provide automated sterilization during off-hours.
Access ControlRFID card readers or biometric systems ensure personalized access. Automated logging records every cabinet opening with timestamps for FDA audits and regulatory compliance.
Case StudyA Russian pharmaceutical facility implemented our cabinets in ISO Class 5 areas. Over two years of operation, zero contamination incidents related to footwear were recorded. Regulatory inspection passed without observations.
5-year warranty, 20+ years service life. Choose reliability and global standard compliance!Laboratory shoe cabinets are critical components in contamination control strategies for cleanrooms and safety areas. Our specialized solutions serve pharmaceutical manufacturing, biotechnology laboratories, and healthcare institutions.
Standards ComplianceOur shoe cabinets meet ISO 14644 requirements for cleanroom classifications 5-8 and GMP guidelines. Designed in accordance with FDA 21 CFR Part 11 for electronic records and sterile manufacturing environments.
Material ConstructionCabinet bodies are fabricated from AISI 304 or 316L stainless steel with electropolished surfaces achieving Ra ≤ 0.4 μm roughness. All corners feature radius ≥ 50 mm to eliminate cleaning dead zones. TIG welding creates seamless joints.
Contamination Barrier DesignCabinets employ strict zoning separating "dirty" and "clean" areas. Dual-compartment configuration with physical barriers prevents cross-contamination between non-sterile and sterile surfaces.
Ventilation SystemsIntegrated HEPA H14 filtration provides continuous air exchange, maintaining ISO Class 7 conditions internally. Optional UV-C germicidal lamps (254 nm) provide automated sterilization during off-hours.
Access ControlRFID card readers or biometric systems ensure personalized access. Automated logging records every cabinet opening with timestamps for FDA audits and regulatory compliance.
Case StudyA Russian pharmaceutical facility implemented our cabinets in ISO Class 5 areas. Over two years of operation, zero contamination incidents related to footwear were recorded. Regulatory inspection passed without observations.
5-year warranty, 20+ years service life. Choose reliability and global standard compliance!
