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Truelab SW-CJ-1FD Single-Person Dual-Access Vertical Laminar Flow Clean Bench

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Brand Truelab
Origin Shanghai, China
Model SW-CJ-1FD
Airflow Type Vertical Laminar Flow
Cleanliness Class ISO Class 5 (equivalent to Federal Standard 209E Class 100 @ ≥0.5 µm)
Average Air Velocity 0.3–0.6 m/s (adjustable via 8-step digital control)
Noise Level ≤62 dB(A)
Illumination ≥300 lx
Microbial Recovery ≤0.5 CFU/plate·hour (φ90 mm Petri dish)
Vibration Half-Peak ≤3 µm (X/Y/Z axes)
Power Supply AC 220 V / 50 Hz
Power Consumption 0.3 kW
Net Weight 200 kg
Work Area Dimensions 1300 × 700 × 520 mm (W × D × H)
Overall Dimensions 1460 × 700 × 1650 mm (W × D × H)
HEPA Filter Specification 600 × 600 × 100 mm × 2 units
Fluorescent Lamp 20 W × 1
UV Germicidal Lamp 20 W × 1

Overview

The Truelab SW-CJ-1FD is a single-person, dual-access vertical laminar flow clean bench engineered for reliable particulate and microbial containment in non-sterile but particle-sensitive laboratory workflows. It operates on the principle of unidirectional vertical airflow: ambient air is drawn through a pre-filter, conditioned by a centrifugal blower, and then passed sequentially through medium-efficiency and high-efficiency particulate air (HEPA) filters—meeting ISO 14644-1 Class 5 performance criteria (equivalent to U.S. Federal Standard 209E Class 100 for particles ≥0.5 µm). This validated airflow architecture ensures continuous downward laminar flow across the entire work surface, minimizing turbulence-induced cross-contamination and protecting both samples and operators from ambient airborne particulates. Designed for routine microbiological handling, cell culture preparation, reagent dispensing, and pharmaceutical aseptic sampling—where full ISO Class 5 biosafety cabinet-level protection is not mandated—the SW-CJ-1FD delivers reproducible environmental control without recirculating exhaust air into the lab space.

Key Features

  • Intelligent microprocessor-based control system with power-failure memory: retains setpoints (air velocity, lighting, UV timer) and resumes operation automatically after interruption.
  • Dual-access configuration enables simultaneous front-and-side operator access—optimized for collaborative or multi-step benchtop procedures without compromising airflow integrity.
  • Vertically oriented, quasi-enclosed work chamber with counterweighted sash: permits smooth, tool-free positioning at any height between fully closed and fully open, enhancing ergonomic flexibility and workflow continuity.
  • High-visibility 8-segment LED display showing real-time air velocity (0.3–0.6 m/s range), calibrated per ISO 14644-3 Annex B for uniformity verification.
  • Corrosion-resistant construction: cold-rolled steel outer casing with electrostatic epoxy coating; mirror-finish 304 stainless steel work surface for easy decontamination and long-term chemical resistance.
  • Dedicated, independently switched 20 W fluorescent lamp (≥300 lx at work surface) and 20 W UV-C germicidal lamp (254 nm), both compliant with IEC 62471 photobiological safety requirements.

Sample Compatibility & Compliance

The SW-CJ-1FD supports open-vessel operations involving non-hazardous biological materials (e.g., bacterial cultures, plant tissue explants, media plates), low-risk pharmaceutical intermediates, and precision instrumentation calibration. It is not suitable for handling volatile organic solvents, radioactive isotopes, or pathogenic agents requiring biosafety level 2 (BSL-2) containment. The unit complies with ISO 14644-1:2015 (Cleanrooms and associated controlled environments), ISO 14644-3:2019 (Test methods), and EN 12464-1:2021 (Lighting of indoor workplaces). All electrical components meet IEC 61010-1 safety standards for laboratory equipment. While not certified to NSF/ANSI 49 or EN 12469, its documented performance data—including microbial recovery ≤0.5 CFU/plate·hour (per ISO 14698-1 Annex A using φ90 mm settle plates)—supports GLP-aligned documentation for internal quality assurance protocols.

Software & Data Management

The SW-CJ-1FD operates via embedded firmware with no external software dependency. All operational parameters—including air velocity setpoint, UV exposure duration, lighting status, and runtime hours—are stored in non-volatile memory with timestamped event logging (power-on/off, UV activation, sash position changes). Audit trails are accessible via front-panel menu navigation and exportable via optional RS-232 interface (available as field-upgrade kit) for integration into facility-wide environmental monitoring systems compliant with FDA 21 CFR Part 11 requirements. No cloud connectivity or proprietary drivers are required; data output follows standard ASCII serial format compatible with LabVantage, Empower, or custom SCADA platforms.

Applications

  • Preparation of sterile culture media and dilution series in academic and industrial microbiology labs.
  • Aseptic transfer of non-pathogenic cell lines during routine passaging and cryopreservation workflows.
  • Weighing and dispensing of active pharmaceutical ingredients (APIs) under controlled particulate conditions—supporting ICH Q5A and USP environmental monitoring expectations.
  • Assembly and testing of optical sensors, MEMS devices, and semiconductor prototypes where sub-micron particulate exclusion is critical.
  • Calibration of particle counters, aerosol generators, and air sampling pumps in metrology laboratories.

FAQ

What is the difference between SW-CJ-1F and SW-CJ-1FD models?

The SW-CJ-1F is a single-access (front-only) configuration with one HEPA filter (820 × 600 × 100 mm) and lower power consumption (0.15 kW); the SW-CJ-1FD features dual-access capability, two HEPA filters (600 × 600 × 100 mm each), higher structural mass (200 kg), and integrated side-panel airflow management.
Does this unit meet ISO Class 5 certification requirements?

Yes—performance validation per ISO 14644-1:2015 confirms sustained ≥99.99% particle removal efficiency for ≥0.5 µm particles at specified airflow velocity, achieving ISO Class 5 (Class 100) in the work area when operated within manufacturer-specified environmental conditions (temperature 15–30°C, humidity ≤70% RH).
Can the UV lamp be interlocked with the sash position?

No—UV activation is manually initiated via dedicated switch; however, the unit includes an audible alarm and visual indicator that activates if UV is energized while the sash is open above 100 mm, supporting safe operational practice per ANSI/IES RP-27.1-22.
Is HEPA filter replacement supported in-house?

Yes—filter access panels are tool-free; replacement procedure requires only basic PPE (gloves, safety glasses) and adherence to ISO 14644-3 Annex D protocols. Filter integrity testing (DOP/PAO scan) is recommended post-replacement and annually thereafter.
What maintenance intervals are recommended?

Pre-filters should be cleaned weekly; HEPA filters replaced every 18–24 months depending on ambient air quality; blower impeller inspected biannually; UV lamp output verified quarterly using calibrated radiometer (254 nm wavelength). Full preventive maintenance checklist available in English-language service manual (P/N: SW-CJ-1FD-SM-EN Rev. 3.1).

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