Electric Lift Pass Box LELP-T2010

Introduction

Electric features a channel size of 680mm×570mm×560mm, medium-sized dynamic pass box dimensions that accommodate common trays. It is built from 304 stainless steel and is sealed with high-clarity tempered glass. The system has integrated with a UV‑C germicidal lamp with a timer for optional microbial sterilization. Our electric lifting pass box includes a stage filtration mode that removes larger and finer particles sequentially.

This pass box is designed to meet the rigorous requirements of modern laboratory operations, ensuring high precision, reliability, and ease of use for various experimental applications.

Applications

Electric Lifting Passing Box serves as a sealed, motorized transfer chambers that block air convection and contamination. It plays a key role in pharmaceuticals, biotechnology, electronics, and semiconductor manufacturing for the efficient transfer of materials.

Specifications

Control Mode	One-button lifting / foot pedal lifting
Interlocking Function	Standard
Intercom Function	Standard
Anti-Pinch Function	Touch rebound + infrared sensors
Motor Power	25W
Ultraviolet Power	5W
Total Power	30W
Power Supply	AC / 220
Channel Size	680mm × 570mm× 560mm
Dimensions	900mm × 700mm × 1200mm

Features

Motorized Lift Mechanism

Interlocked Safety System

Infrared Anti‑Pinch Sensors

Built‑in Intercom Communication

UV Sterilization Mode 

FAQs

1. How does the dual-stage filtration system enhance clean-air performance in electric lift pass box ?

Electric lift pass box uses both a pre-filter (EU6/EU7) and a filter (H13/H14) to sequentially eliminate large and fine particulates, achieving over 99.97% efficiency at 0.3?µm. The pre-filter traps coarse dust, thereby extending life, while the filter ensures Class 5 air quality. A centrifugal motor-blower draws air through the filters and distributes it evenly into the chamber, maintaining laminar flow at 0.45?±?0.05?m/s. Continuous differential pressure monitoring ensures both filters are within operating thresholds. This staged approach preserves airflow quality while enabling fewer filter replacements and lower maintenance costs.

2. Can I use the electric lift pass box in potentially explosive or hazardous environments?

Yes, many models of electric lift pas box offer - or flame-proof variants, featuring explosion-proof motors, sealed wiring, and conductive finishes. These comply with safety standards for Zone 1 or Zone 2 hazardous areas, preventing ignition from sparks or static discharge. The body is typically stainless steel and grounded to reduce static buildup. Specialized interlocks and sensors are rated to operate even under explosive atmosphere conditions. Compliance with certification protocols ensures safe use in chemical and pharmaceutical settings. It’s possible to request specific ratings and certificates from vendors to match site hazard classifications.

3. How do touchscreen controls improve operation and auditability in electric lift pass box ?

It supplies advanced models of Electric Lift Pass Box .Touchscreen panels elevate usability and traceability by allowing touch-, password-, or level-access controls for settings like UV timers, blower run time, door-release delays, and alarms. They can record operational cycles, log filter changes, and auto-reset UV-hour counters. In some systems, two-tier access (operator vs. supervisor) restricts critical settings from unauthorized users. The data history supports DQ/IQ/OQ/PQ documentation and simplifies compliance reporting under guidelines. Touchscreens also reduce wear and contamination risk compared to mechanical switches.

4. What are non-visual maintenance indicators to note in ?

It supplies advanced models like Electric Lift Pass Box .Apart from visible alarms and lights, the system includes audio beeps for door-hold, blower failure, or UV lamp issues, as well as vibration sensors in motor-blowers to detect bearing wear. Magnehelic gauges may include alarms if the pressure differential crosses set thresholds. Blower current sensing can indicate motor failure or filter clogging. Some models even send remote alerts via systems. These feedback systems enable maintenance without opening the chamber or waiting for visual cues.

5. How customizable are size, orientation, and transfer options in Electric Lift Pass Box ?

It supplies premium electric lift pass box . Manufacturers offer a range of standard interior sizes and can produce L-shaped, multi-door, or stacked two-floor configurations. Wall-, floor-, and flush-mount styles adapt to various cleanroom partitions. Accessories like intercoms, pressure gauges, UV disinfection, ports, and flame-proof fittings can be integrated. Blower types range from AC to EC/DC with variable-speed drives. For unique applications-like drum transfers or high-throughput labs-custom dimensions and features are routinely engineered to order.

6. What is the working principle of a dynamic Electric Lift Pass Box?

It employs a filtered airflow system where a built-in fan recirculates air vertically or horizontally through filters, maintaining Class 5 cleanliness inside the chamber. When the lift activates, purified air enters the compartment to dilute particles from transferred items and returns via a grille—creating a continuous clean-air cycle. Dual-stage filtration (pre-filter + H13/H14 ) removes both large and fine contaminants. Differential pressure monitoring ensures filter performance, while the air velocity is typically maintained. These continuous airflow dynamics keep the internal chamber sterile during the lifting process.

7. How do the interlock and alarm systems enhance safety and compliance?

The unit features electronic or electromagnetic interlock mechanisms that strictly prevent both doors from being opened simultaneously, effectively stopping cross-contamination. Fan operation locks the doors, and opening a door usually triggers an automatic UV shut-off and -visual indicators. In addition, digital or analog differential pressure gauges with alarm thresholds alert when pressure deviates, signalling filter clogging or malfunction. Audio-visual alarms can also be set to notify operators of extended door openings or blower issues, ensuring compliance with / protocols.

8. What maintenance and monitoring routines are required to ensure optimal performance?

Regular maintenance includes replacing the pre-filter every 1 to 6 months and the filter every 6 to12 months, depending on usage and particle load. After filter replacement, integrity tests using particle counters or / ports ensure there’s no leakage. Periodic airflow visualization (e.g., smoke test) confirms unidirectional flow. Daily or monthly differential pressure checks validate proper ventilation performance. UV-C lamps and internal chamber surfaces are cleaned weekly using approved disinfectants. Power components should be handled cautiously, with non-professional personnel restricted from circuit board access.

9. Can these units accommodate different cleanroom classifications and hazardous environments?

Yes—dynamic pass boxes are engineered to support transfers between various -grade environments (e.g., non-clean to 5 or C to B), acting as airtight airlocks. Some models are available in explosion-proof/-rated variants for use with combustible or hazardous materials. The airflow system is designed with variable-frequency drives to maintain consistent differential pressure, even if both doors are opened briefly. Configuration options include single-, double-, L-shaped, or multi-sided designs tailored for compartment-specific layout. Accessories like UV-C disinfection, intercom systems, and touchscreen panels increase flexibility across pharmaceutical, biotech, and industrial applications.

10. How do built-in monitoring features support regulatory compliance?

Equipped with differential pressure gauges (analog /digital), the pass box continually monitors filter loading and airflow performance—providing data for maintenance logs. / test ports allow onsite filter integrity testing, essential for validation. Door completion timers and UV-hour meters track usage cycles and UV exposure durations, enabling routine documentation. Control systems often include password-protected or touchscreen interfaces for secure adjustments. Together, these systems support full lifecycle documentation—DQ/IQ/OQ/PQ protocols—and help satisfy audit requirements under 14644, , US cGMP, and guidelines.