Introduction
A xenon light pass box combines material transfer with UV sterilization using xenon light. It is widely used in pharmaceutical cleanrooms. The system ensures sterilized transfer. It solves microbial contamination risks. By integrating light sterilization, it supports aseptic environments.
Xenon Light Pass Box LXLP-T2011
Xenon offers a spore killing efficiency of ≥99.9% spore‑kill xenon light pass box for contamination‑free cleanroom transfers. It provides UV shielding safeguards operators for operati...
Xenon Light Pass Box LXLP-T2010
Xenon features a material passing time ≤3 using high-intensity pulsed xenon UV light to ensure rapid disinfection. The system has an integrated deozonation module for removing any ozone...
Standards
ISO 14644-1-Cleanrooms and associated controlled environments-Classification of air cleanliness by particle concentration
ISO 14644-3-Cleanrooms and associated controlled environments-Test methods
Complies with the above standards, but is not limited to them.
Features
1. Airflow monitor or alarm indicates filter and fan status.
2. UV sterilisation option is available on selected models.
3. Clear work zone with good visibility and integrated lighting.
4. Smooth stainless or steel surfaces are easy to clean.
5. HEPA filtration provides clean, controlled airflow over the work area.
FAQ
What are the main applications of the Xenon Light Pass Box?
The Xenon Light Pass Box is used to provide clean or controlled airflow for handling samples, powders or operations that need protection from contamination or airborne exposure. It supports pharmaceutical, microbiological, analytical and electronics work.
What standards does the Xenon Light Pass Box comply with?
The unit is designed with reference to IEC 61010 electrical safety, applicable clean-air and containment standards and relevant GB/T methods. Filters and airflow should be tested periodically. Compliance documentation can be provided on request.
What warranty comes with the Xenon Light Pass Box?
A 12-month warranty applies to the complete equipment against defects in materials and workmanship. It excludes consumables, wearing components and accidental or misuse damage. Our service team handles claims against the serial number, and longer cover can be arranged.
Will staff need special training?
Routine operation is straightforward and is covered in the user manual, including setup, daily use and basic maintenance. Staff with basic laboratory experience can run it after a short familiarisation. We provide remote guidance and can arrange on-site training where required.
What is the typical lead time for order delivery?
Standard models require 7-30 working days. In-stock units can ship within 3-7 working days. Custom configurations or large built-to-order systems may require additional time, and we confirm the exact schedule before order confirmation.
How often should the Xenon Light Pass Box be calibrated?
To protect result reliability, periodic verification should be performed, typically once or twice a year. The instrument arrives factory-calibrated, and self-check routines help spot drift. We offer traceable calibration service if the site needs it.
Are consumables and spare parts easy to obtain?
No proprietary consumable contract is required; standard parts are available from us and common laboratory suppliers. Our service team can supply a recommended parts list for the model. Most routine spares are held for quick delivery.
Are options or configurations available?
Yes, common options include different ranges, voltages, accessories, interfaces and capacity or size configurations. We confirm feasibility, specifications and any delivery impact before order confirmation. Custom requirements are reviewed case by case.
Is installation and commissioning included?
Benchtop and standard units typically require only placement and connection before use, while larger systems may need professional commissioning. We confirm the installation requirements at order stage. On-site service and training can be provided if needed.
What maintenance and safety points matter?
Do not handle highly toxic or pathogenic agents beyond the containment class, block the face opening or rely on expired filters. Verify airflow and filter integrity. Follow laboratory safety rules.
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