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| Categories | Clean Room Pass Box |
|---|---|
| Brand Name: | MRJH |
| Certification: | ISO.GMP.CE.UL |
| MOQ: | 1 |
| Price: | Contact Us |
| Delivery Time: | 7-15 working days |
| Company Info. |
| Shenzhen Meiri Purification Technology Co., Ltd. |
| Verified Supplier |
| View Contact Details |
| Product List |

| Parameter | Specification |
|---|---|
| Structure | Dual-layer stainless steel chambers |
| Interlock System | Electronic sensor control (fail-safe logic) |
| Material | 304 Stainless steel / Powder-coated steel |
| Viewing Window | Double-layer tempered glass (5-8mm thickness) |
| Sealing | EPDM gasket (ISO Class 4~8 compatible) |
| Control Panel | Touchscreen HMI with cycle log & alarm |
| Safety | UV sterilization option / Pressure equalization port |
| Size Options | Customizable (e.g. 600×600×800mm) |
Advanced Dual-Chamber Barrier Technology
Our Double-Door Electronic Interlock Pass-Through ensures zero
cross-contamination during material transfer between controlled
environments. The intelligent electronic interlock system prevents
simultaneous door opening through sensor-based automation, while
dual independent chambers create a physical isolation zone.
Featuring real-time status monitoring and configurable purge cycles (air shower/vacuum/UV), it maintains ISO 14644-1 compliance for critical sectors like pharmaceuticals and microelectronics. The robust 304 SS construction with seamless welds eliminates particle traps, and the intuitive HMI allows audit trail export for GMP documentation.
Pharma Labs
Transfer vials between Grade B/C cleanrooms
Biotech Facilities
Sample movement in BSL-2/3 laboratories
Electronics Manufacturing
Wafer handling in semiconductor fabs (Class 100-1000)
Hospitals
Pharmacy-to-ward sterile supply transfer
Food Production
Raw material entry to HACCP zones








Q1: How does the double-chamber design prevent cross-contamination
compared to single-door pass boxes?
*A: Unlike conventional pass-throughs, our dual-chamber system
creates a physical isolation zone between environments:
Stage 1: Outer door opens → material enters first chamber → door seals
Stage 2: Internal sensors validate cleanliness → inner door unlocks
Critical Safeguard: Electronic interlock enforces <2% door overlap risk (per EN
12469) via infrared sensors.
This sequential transfer protocol blocks >99.97% of airborne
particles (tested per ISO 14644-3).*
Q2: What certifications support compliance with pharmaceutical
regulations?
*A: The system is engineered for full traceability:
GMP Compliance: Validatable per EU GMP Annex 1 (2022) & FDA 21 CFR Part 11 (electronic records)
Safety Certificates: CE-marked with SIL-2 rated interlocks (IEC 61508)
Material Traceability: 304 SS material certificates & EPDM gasket USP Class VI reports included
Audit Support: HMI stores 25,000+ event logs with CSV export for regulatory audits.*
Q3: Can it integrate with existing cleanroom control systems?
*A: Yes, we offer flexible integration:
Communication: Modbus RTU/TCP protocol for BAS/BMS connectivity
Automation: Dry-contact signals for door status/errors to SCADA
Customization: Optional pressure sensors (0-30 Pa) for differential pressure monitoring
Upgrade Path: Firmware supports future ISO 14644-18:2022 updates.
(Note: Provide cleanroom class & PLC type for pre-configuration)*
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