Deiiang Laboratory Furniture Equipment Product Catalog is a comprehensive product reference document that details Deiiang’s full portfolio of professional laboratory furniture and equipment — including fume hoods, lab workbenches, chemical storage units and safety fixtures — with complete technical specifications and customizable solutions for scientific research, pharmaceutical, industrial testing and cleanroom laboratory applications.

SIST EN 14175-3:2019 is the Slovenian national adoption of European standard EN 14175-3:2019, which specifies formal type test methodologies to verify the fume containment safety and operational performance of laboratory fume cupboards connected to dedicated exhaust air systems, as the testing complement to the mandatory performance requirements defined in EN 14175-2.

EN 17242:2025 is a European standard for recirculatory filtration fume cabinets (RFFCs) that specifies uniform design, manufacturing, type testing and on-site testing requirements, to ensure effective containment and filtration of hazardous airborne contaminants before exhaust air is recirculated back into the laboratory, and harmonizes safety performance benchmarks for filtered fume enclosures across Europe.

EN 12792:2003 is a European standard that defines unified terminology, measurement units, and graphical symbols for building ventilation and air-conditioning systems, providing a consistent lexical and visual reference for all ventilation-related European standards and engineering practices.

ANSI/ASSP Z9.5-2022 is an American National Standard focused on laboratory ventilation, which establishes minimum requirements and industry best practices for ventilation system design, fume hood performance testing, and formal Laboratory Ventilation Management Plans, to protect laboratory personnel from physical harm and overexposure to hazardous airborne contaminants.

The OSHA Laboratory Standard (29 CFR 1910.1450) is a U.S. federal occupational safety regulation that protects laboratory workers from health hazards caused by exposure to hazardous chemicals, by requiring laboratories to establish a written Chemical Hygiene Plan and implement corresponding safety training, exposure monitoring and risk control measures.

SIST EN 16611:2023 (EN 16611:2023) specifies methods and test procedures for assessing the surface resistance of furniture to microscratching and evaluating surface durability. ([sis.se](https://www.sis.se/en/produkter/domestic-and-commercial-equipment-entertainment-sports/furniture/ss-en-166112023/?utm_source=openai))

EN 61010 specifies safety requirements for electrical equipment for measurement, control, and laboratory use to protect users and property from electrical, mechanical, and thermal hazards.

ISO 846:2019 specifies laboratory methods for evaluating the resistance of plastics to the action of microorganisms (fungi and bacteria) under controlled conditions.

ISO 16232 specifies test methods for assessing particulate contamination (particle extraction, counting, sizing, and analysis) on components of fluid systems in road vehicles to ensure cleanliness and performance.

ISO 14644-9:2022 specifies methods for assessing and classifying the cleanliness of surfaces in cleanrooms and associated controlled environments based on particle concentration. ([iso.org](https://www.iso.org/standard/76889.html?utm_source=openai))

ISO 14644-7:2004 specifies classification, design, testing, and operational requirements for separative devices (isolators, minienvironments, clean air hoods and suits) used to provide localized controlled environments.

ISO 14644-5 provides requirements and recommendations for the operation of cleanrooms and associated controlled environments, covering procedures for cleaning, maintenance, personnel, gowning, and monitoring to maintain contamination control.

ISO 14644-4:2022 provides international requirements and guidance for the design, construction, and start-up of cleanrooms and associated controlled environments to ensure they meet contamination control and performance criteria.

ISO 14644 defines the standards for cleanrooms and associated controlled environments, covering their classification by air cleanliness, design, operation, monitoring, and testing to ensure effective contamination control.

SIST EN 16611:2023 specifies performance requirements and test methods for air filters used in general ventilation, focusing on their efficiency, pressure drop, and suitability for indoor air quality and energy-efficient HVAC applications.

EN 779 specifies a test method and classification system for particulate air filters used in general ventilation, rating their performance based on particle removal efficiency and pressure drop.

ISO 16890-3:2016 specifies test procedures for determining the gravimetric efficiency and air flow resistance of air filters for general ventilation, supporting their classification based on particulate matter size fractions.

SIST EN 1822-2:2010 defines aerosol production, measuring equipment, and testing methods used to determine the efficiency and classification of high-efficiency air filters (HEPA/ULPA) in cleanroom and contamination control applications.

SIST EN 1822-4:2001 specifies the test methods and requirements for determining local filter efficiencies and leakages of high-efficiency air filters (HEPA/ULPA), ensuring reliable performance in critical cleanroom and contamination control applications.

ISO 16890:2022 establishes a test and classification system for air filters used in general ventilation, rating their efficiency based on particulate matter size fractions (PM1, PM2.5, and PM10) to better reflect real-world outdoor air conditions.

ISO 16889:2022 specifies a multi-pass test method for evaluating the performance of filters used in hydraulic fluid power systems, including particle removal efficiency and dirt-holding capacity under defined operating conditions.

ASHRAE 52.2 specifies the method of testing air-cleaning filters for ventilation air, providing Minimum Efficiency Reporting Values (MERV) to rate filter performance by particle size and removal efficiency.

EU GMP Annex 15 (2015) provides detailed guidance on qualification and validation for pharmaceutical manufacturing, covering equipment, facilities, utilities, processes, and cleaning to ensure consistent product quality and regulatory compliance.

USP <800> establishes standards for the safe handling of hazardous drugs to protect healthcare workers, patients, and the environment through appropriate facility design, engineering controls, and work practices.

This document provides detailed technical information, specifications, and application guidelines to support the correct selection, design, and use of the referenced cleanroom-related product or system.

EU GMP Volume 4 Annex 1 (2022) sets out detailed regulatory requirements and guidance for the manufacture of sterile medicinal products, focusing on contamination control, cleanroom classification, and robust aseptic processing.

Federal Standard 209 defines the classification of cleanrooms based on airborne particulate cleanliness, providing foundational criteria for designing, operating, and validating controlled environments.

Deiiang Laminar Flow Hoods provide ultra-clean, unidirectional airflow with low noise and stable performance, ensuring reliable product protection and contamination control in critical work areas.

Deiiang Downflow Booth provides a controlled, vertical laminar airflow zone that efficiently captures and removes contaminants, ensuring operator safety, product protection, and a clean working environment.

Deiiang FFU delivers high-efficiency, low-noise laminar airflow with stable performance and easy integration, providing reliable clean air protection for critical environments.

Our HVAC air filters deliver high-efficiency particulate removal, low pressure drop, and reliable protection for clean, healthy, and energy-efficient indoor environments.

Deiiang's pass-through window series includes static and dynamic models, fully compliant with GMP and ISO14644 standards, and sizes are customizable.

IEST-RP-CC026 is an industry recommended practice that provides guidelines and best practices for the operation and management of cleanrooms and other controlled environments.

A collection of Deiiang cleanroom project case studies, visually showcasing the overall completed cleanroom results.

Deiiang cleanroom-specific PVC flooring is made of homogeneous material, making it durable, comfortable underfoot, and can be treated with anti-static agents upon request.

Deiiang's air showers are fully automatic and sensor-operated, with nozzle airflow speeds of 30m/s. This effectively removes dust particles adhering to people and goods, ensuring a safe and healthy cleanroom environment.

Deiiang's cleanroom-specific observation window features double-layer insulation, inert gas flushing to prevent fogging, an internal stainless steel frame, and an elegant design. It has passed UL and CE certification tests.

Designed by Deiiang experts, these doors meet international cleanroom standards, support GMP compliance, and enhance the safety, durability, and energy efficiency of pharmaceutical, biotechnology, electronics, and medical environments.

Deiiang's cleanroom-grade aluminum profiles are sturdy, durable, easy to clean, and available in various colors and styles including natural, electrophoretic, and anodized aluminum. They meet GMP and FDA certification standards.

Explore Deiiang Cleanroom Panels Systems engineered for airtight performance, durability, and GMP-compliant cleanliness across critical environments.

Deiiang Construction has been plowing into the field of engineering construction for more than 20 years, and is a leading EPC service provider in the field of high-tech industrial construction in China

Cleanrooms and associated controlled environments — Part 1: Classification of air cleanliness by particle concentration

Cleanroom design specifications define the structural, airflow, filtration, and cleanliness requirements needed to control contamination in a controlled environment.