Professional Clean Environment Ensuring Accurate and Safe Pathological Testing
The Pathology Department Cleanroom is a modular clean environment specifically designed for hospital pathology labs, CDC facilities, and research institutions. It meets the high-standard operational requirements for pathological sample processing, slide preparation, molecular testing, and more. Through precise temperature and humidity control, air purification, and airflow management, it effectively prevents cross-contamination of samples, ensuring the accuracy and reliability of test results.
Category | Parameter | Technical Specification | Remarks |
Basic Parameters | Cleanliness Class | ISO Class 5-8 (Class 100 to Class 100,000) | Customizable to Class 4 |
Structure Type | Modular assembly (wall/ceiling/floor panels) | Quick installation | |
Main Material | 304 stainless steel/electrolytic steel plate (anti-static coating) | Corrosion-resistant | |
Environmental Control | Temperature Range | 20-26°C ±1°C | Intelligent temperature control |
Humidity Range | 45-65% RH ±5% | Auto-regulated | |
Pressure Control | ±5-20 Pa adjustable | Zonal pressure gradient | |
Air Changes | 15-60 ACH | Adjustable by cleanliness class | |
Air Handling | Filtration System | Pre-filter G4 + HEPA H13/H14 | 99.97%@0.3μm efficiency |
Airflow Pattern | Unidirectional vertical/horizontal flow | FFU coverage ≥30% | |
Recovery Time | ≤15 min (ISO 8→5) | ||
Safety Features | Biosafety | Optional negative pressure system (-10~-30 Pa) | Pathogen containment |
Electrical Safety | Explosion-proof lighting/sockets | Complies with GB50073 | |
Disinfection Compatibility | Resistant to ozone/hydrogen peroxide fumigation | ||
Functional Configurations | Pass-through | Interlocked stainless steel pass-through with UV sterilization | Custom sizes available |
Smart System | Real-time monitoring (temp/humidity/pressure/particles) | Data logging & traceability | |
Emergency Equipment | Emergency lighting/shutdown system | Optional emergency shower | |
Certifications | Compliance | Meets GMP/GLP, WS 233-2017 "Biosafety in Pathogen Laboratories" | Validation documents provided |
FAQ:
1. What is the lead time for a modular cleanroom?
The lead time depends on the size, customization, and cleanroom class. Standard configurations typically take 2–4 weeks for production and 1–2 weeks for installation. Custom designs (e.g., ISO Class 4, specialized materials) may require 6–8 weeks. We provide a detailed timeline after evaluating project requirements.
2. Can the cleanroom be relocated or expanded later?
Yes! Modular cleanrooms are designed for flexibility. Walls, ceilings, and filtration systems can be disassembled and reinstalled at a new site. Expansion is seamless—additional modules integrate with existing structures without compromising cleanliness. Note: Relocation may require revalidation of ISO/GMP standards.
3. How is air cleanliness maintained during power outages?
Our systems include emergency power options (e.g., UPS/battery backups for FFUs) to sustain airflow briefly. For prolonged outages, we recommend:
* Redundant power supplies (generators).
* Airlocks/positive pressure buffers to minimize contamination.
Post-outage, the cleanroom’s rapid recovery time (≤15 minutes) restores conditions quickly.