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  1. Home
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  3. UL Japan
  4. [Event] Technical Consultation Meeting on Safety Evaluation of Laser Light Emission
SEMINAR_EVENT
  • Apr 03, 2024
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Apr 03, 2024

[Event] Technical Consultation Meeting on Safety Evaluation of Laser Light Emission

UL Japan UL Japan
In recent years, the planned abolition of FDA Laser Notice 50 has been announced in the United States, and in Europe, regulations such as EN 60825-1+A11 and EN 50689 have been issued, leading to significant changes in regulations regarding laser products. Do you have any concerns about compliance with safety standards for laser products being shipped to the U.S. or Europe in relation to these regulations and standards? To address such customer inquiries and concerns, we will hold a free individual consultation session regarding compliance with safety standards for laser products. Our experienced specialists from UL Solutions, which has a 130-year history and leads safety science through a global network, will carefully answer your questions and concerns. You can check the details of the technical consultation session by clicking the "Details & Application" button below.
Date and time Monday, May 13, 2024 ~ Friday, May 17, 2024
Daily 9:30 AM to 4:45 PM (1 session 45 minutes)
Capital
Entry fee Free
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Laser_1.jpg

Laser product safety evaluation services

Technology and achievements that support advanced laser products.

UL provides conformity assessment services for laser product safety requirements in accordance with IEC 60825 and the U.S. FDA (CDRH) based on years of diverse evaluation experience with laser products. This allows manufacturers to verify that their products meet laser-related safety requirements as they enter the global market and obtain the technical documentation to support this. We encourage you to consider utilizing UL's laser product safety evaluation services. ■ IEC 60825 Evaluation UL is accredited as a CB testing laboratory for the international standard on laser safety, IEC 60825-1/-2. <Services Offered> - Determination of laser class for laser products - Safety evaluation of laser products ■ Support for U.S. FDA CDRH Laser Product Report Preparation Manufacturers selling laser products in the U.S. market are obligated to comply with FDA requirements and submit a Laser Product Report (and other required reports) to CDRH under U.S. federal regulations. <Services Offered> - Verification of FDA requirement compliance for laser products and preparation of CDRH Laser Product Report.

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LED_FAQ.jpg

Brochure "Q&A on the Photobiological Safety of LED-Equipped Products"

What are the requirements for the photobiological safety of products equipped with LEDs? We answer questions like this!

This booklet answers questions regarding the safety of LED radiation in a Q&A format. What are the requirements for the photobiological safety of products equipped with LEDs? How is the potential hazard of LED radiation from products expressed? How are the risk groups for LED radiation determined? These topics are covered. [Excerpt of Contents] ■ What are the requirements for the photobiological safety of products equipped with LEDs? ■ How is the potential hazard of LED radiation from products expressed? ■ Can radiation from lamps other than LEDs also be evaluated for photobiological safety? ■ How are the risk groups for LED radiation determined? *For more details, please refer to the PDF document or feel free to contact us.

  • LED Module

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レーザーFAQ.jpg

Booklet "Q&A on Safety Standards for Laser Products"

How is the class of a laser determined? We are answering questions like this!

This booklet answers questions about laser safety in a Q&A format. It includes topics such as what the safety requirements for laser products are, how the class of a laser is determined, and how to know if the laser radiation emitted from a product is hazardous. Additionally, the classification of lasers is explained clearly using tables. 【Contents (excerpt)】 ■ What are the safety requirements for laser products? ■ How is the potential hazard of lasers from products represented? ■ How is the class of a laser determined? ■ How can we know if the laser radiation emitted from a product is dangerous? *For more details, please refer to the PDF document or feel free to contact us.

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VM_1.jpg

Third-party verification of lasers/LEDs

UL Verified Mark - You can promote the safety of light radiation.

Laser and LED technologies are applied in various fields such as information technology, healthcare, entertainment, and the automotive industry. With the increase in products, manufacturers are pressured to differentiate their products in the market. On the other hand, for consumers, the incorporation of lasers and LEDs into more familiar products has made safety assurance an important factor in product selection. In this era, UL's Verified Mark is the optimal program to appeal to buyers regarding the safety of laser/LED light emission levels in products. Why is verification necessary? The UL Verified Mark program for laser/LED products is a third-party verification service aimed at verifying the emission levels of lasers/LEDs at reliable testing laboratories and utilizing the results in your marketing activities. By using it alongside UL's well-recognized safety evaluation services in the United States, it alleviates concerns for users and retailers while promoting brand transparency in the market. Products that measure laser/LED emission levels are categorized into three groups under this unique UL program.

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U.S. FDA/CDRH Safety Standards and Registration (Notification) for Laser Products

We will provide a clear explanation of the regulations and safety standards that manufacturers must adhere to when importing and selling laser-equipped products in the United States.

In the United States, there are safety regulations regarding radiation exposure for products equipped with lasers. Manufacturers must ensure compliance with safety standards and complete the necessary procedures with the authorities when importing and selling laser products in the U.S. This seminar will explain the safety standards required and the procedures to be followed with the authorities when launching products in the U.S. market.

  • Contract measurement

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LED_1.jpg

LED/Lamp Biochemical Safety Evaluation Service

Technology and achievements related to LED products.

■IEC 62471 Evaluation UL is accredited as a CB testing laboratory for the international standard IEC 62471 concerning the photobiological safety of LEDs and lamps. We offer the following services based on the requests of manufacturers. <IEC 62471 Risk Group Determination for LEDs / Lamps> - We measure the spectral irradiance and spectral radiance of LEDs / lamps to determine the risk group for various hazards. - Deliverable: IEC 62471 evaluation report (using IECEE Official Test Report Form) - Accurately understanding the risk group of the radiation that can be exposed from the installed LEDs / lamps and the product is the first step in ensuring the safety of products equipped with LEDs / lamps.

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Related catalog(6)

Safety evaluation services for laser / LED products

Safety evaluation services for laser / LED products

CATALOG
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Brochure "Q&A on the Photobiological Safety of Products Emitting Ultraviolet Light"

Brochure "Q&A on the Photobiological Safety of Products Emitting Ultraviolet Light"

TECHNICAL
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Booklet "Q&A on the Photobiological Safety of LED-Equipped Products"

Booklet "Q&A on the Photobiological Safety of LED-Equipped Products"

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Booklet "Q&A on Safety Standards for Laser Products"

Booklet "Q&A on Safety Standards for Laser Products"

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Information on reliability evaluation services for automotive LED and laser products.

Information on reliability evaluation services for automotive LED and laser products.

PRODUCT
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[On-Demand Seminar] U.S. FDA/CDRH Safety Standards and Registration (Notification) for Laser Products

[On-Demand Seminar] U.S. FDA/CDRH Safety Standards and Registration (Notification) for Laser Products

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UL Japan
Testing, Analysis and Measurement
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We will exhibit at P-MEC Japan 2025, the Pharmaceutical Ingredients and Equipment Exhibition.

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  • SEMINAR_EVENT

We will be exhibiting at the "P-MEC Japan 2025 Pharmaceutical Ingredients and Equipment Exhibition" held at Tokyo Big Sight. During the event, we will showcase various products. We invite all relevant parties to come and visit us. 【Suppliers】 ・LAUDA

Mar 21, 2026

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25th SMART ENERGY WEEK [Spring]

  • NEW
  • SEMINAR_EVENT

Thank you very much for visiting our booth this time. Thanks to you, we had the opportunity to introduce our products and technologies to many customers, making it a very meaningful time. If you have any questions regarding the exhibition content or if you would like to discuss specific considerations or estimates, please feel free to contact us. We will be happy to provide proposals tailored to your needs.

Mar 20, 2026

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[Seminar] AI Robotics Policy and the Challenges of Two Companies

  • NEW
  • SEMINAR_EVENT

[Lecture Topics] 1. About AI Robotics Tomoya Yokoyama, Section Chief, Robot Policy Office, Industrial Machinery Division, Ministry of Economy, Trade and Industry *The content of the lecture may change. 2. Development of Remote-Controlled Robots Aiming for a Realistic Operating Experience ~Visual and auditory transmission through ultra-low latency, high presence, and high immersion~ Hiroshi Inagaki, Senior Manager, Collaborative Robotics Group, R-Frontier Department, Future Creation Center, Toyota Motor Corporation 3. The Impact of Japanese-Made Humanoids Yasuke Ono, President, Donut Robotics Inc.

Mar 20, 2026

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[Seminar] Value Creation Strategy through Inclusive Design

  • NEW
  • SEMINAR_EVENT

[Speaker] Inclusive Design Designer Yoko Nakao [Key Lecture Content] Products are not selling, differentiation is difficult, and regulations are changing. As product development and facility management reach a significant turning point, inclusive design, which involves engaging people who have previously been excluded from the development process to collaboratively think of solutions, is gaining attention as a method for creating new value. Additionally, practicing inclusive design is expected to enhance not only customer engagement but also employee engagement. In this seminar, based on 20 years of experience leading universal design and inclusive design with diverse characteristics both inside and outside a comprehensive electronics manufacturer, I will specifically explain how to practice inclusive design to create new value. [Lecture Items] 1. Inclusive Design as a New Growth Engine 2. Increasing the Resolution of Diversity 3. Inclusive Design Process 4. Side Effects - Ripple Effects on Talent Development and Recruitment 5. Conclusion 6. Q&A / Business Card Exchange

Mar 20, 2026

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[Seminar] Ministry of Internal Affairs and Communications: Latest Trends in Broadcasting Administration and Future Outlook

  • NEW
  • SEMINAR_EVENT

[Lecture Topics] 1. Future Directions of Broadcasting Policy Reiko Kondo, Director-General for Policy Coordination, Ministry of Internal Affairs and Communications 2. The Nature of Broadcasting Systems in the Broadcasting Era Noriaki Saeki, Director of Broadcasting Policy Division, Ministry of Internal Affairs and Communications 3. Latest Trends in Broadcasting Technology Tomoki Nemoto, Director of Broadcasting Technology Division, Ministry of Internal Affairs and Communications 4. Policy Trends Related to Broadcasting Operations and Future Outlook Toshiyuki Sakairi, Director of Broadcasting Operations Division, Ministry of Internal Affairs and Communications 5. Latest Trends in Maintaining and Strengthening Broadcasting Infrastructure and Facility Development Policy Yukari Iimura, Director of Broadcasting Facility Development Promotion Division, Ministry of Internal Affairs and Communications 6. Latest Trends in Broadcasting and Distribution Content Promotion Policy Hiroki Yoshida, Director of Information and Communication Works Promotion Division, Ministry of Internal Affairs and Communications

Mar 20, 2026

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  • 展示会に出展したいけど準備が大変 展示会の情報をまとめて知りたい そんな展示会のお悩み 展サポで解決! ブース装飾で実績豊富 展示会情報を多数掲載 出展前~後まで支援
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