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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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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"

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

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

OTHER
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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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Notice of participation in "JASIS 2026" from Wednesday, September 2, 2026, to Friday, September 4, 2026.

  • NEW
  • SEMINAR_EVENT

Advantech Toyo will be exhibiting at the trade show "JASIS 2026," which will be held at Makuhari Messe International Exhibition Hall. At this exhibition, manufacturers of analytical and scientific instruments will gather to showcase cutting-edge scientific and analytical systems and solutions. At our booth, we will display filter products for microbiological testing and environmental analysis, water quality testing products, pure and ultra-pure water production equipment, and culture-related equipment. Additionally, we will also showcase analytical balances from Mettler Toledo, along with equipment from other well-regarded manufacturers in the industry. Our sales and technical staff will be available to assist with product selection, so please feel free to stop by!

Aug 20, 2026

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[Seminar] Where does the competitiveness of automobile development differ?

  • NEW
  • SEMINAR_EVENT

[Speakers] Nomura Research Institute, Ltd. Global Manufacturing Consulting Department Group Manager Hirokazu Shimo Senior Consultant Shoki Tokugawa Senior Consultant Wataru Hashimoto Consultant Masaaki Amano Consultant Tomoya Nakamura [Presentation Items] 1. Key Development Themes of Major OEMs 2. Development Approaches of Each OEM 2-1. Toyota 2-2. Tesla 2-3. Suzuki 2-4. Nissan 2-5. Honda 3. Development Approaches of Suppliers 4. Key Points for Strengthening Development Capabilities 5. Q&A / Business Card Exchange

Aug 20, 2026

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[Seminar] Winning Strategies for Telecommunications Carriers in the Era of Physical AI

  • NEW
  • SEMINAR_EVENT

[Speaker] Ayaka Motomura, Consultant, Business Transformation Unit, NTT Data Management Research Institute [Key Lecture Content] With the advancement of Physical AI, telecommunications carriers have the opportunity to evolve from being "companies that provide lines" to companies that connect and control AI and the physical world in real-time. This seminar will organize the changes in communication demand brought about by Physical AI and the business opportunities for telecommunications carriers, while explaining the role of AIOps as the first step towards entry. Furthermore, it will discuss strategies for monetizing in the Physical AI market by deploying the operational intelligence accumulated through AIOps to network APIs and industry-specific services, as well as the layers that telecommunications carriers should hold. [Lecture Topics] Chapter 1: The Competitive Structure of the "Real World" Rewritten by Physical AI Chapter 2: Reasons Why Opportunities for "Reversal" Arise for Telecommunications Carriers in the Era of Physical AI Chapter 3: The First Step Towards Physical AI Chapter 4: Shifting AIOps from "Defense" to "Offense" Chapter 5: The Layers to Hold in the Era of Physical AI [Q&A / Business Card Exchange]

Aug 20, 2026

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[Seminar] Thorough Explanation of the Revised Personal Information Protection Law of Reiwa Year 8

  • NEW
  • SEMINAR_EVENT

[Instructor] Partner Ryoji Mori, Eichi Law Office [Key Lecture Content] This lecture will explain the revised Personal Information Protection Act of 2028. The three-year review this time is a major revision, and it is essential to first understand where and how the revisions have been made, as well as the overall picture of the amendments. Next, we will explain the individual amendments that are practically important. The key points are as follows, but it is important to note that both the strengthening and relaxation of obligations are occurring simultaneously, increasing overall complexity. At the time of the lecture, it is expected that subordinate laws and guidelines will not yet be published, but we will discuss points that require attention upon publication. We will distinguish between what is necessary across businesses and what varies by industry. [Lecture Items] 1. Expansion of consent exceptions: Relaxation of the difficulty of obtaining consent and expansion of academic research institutions 2. Statistical exceptions: System content and how to read complex provisions (plus learning about acceptability from controversies) 3. Strengthening regulations on biometric information and children's information: Caution required for age verification 4. Contactable personal-related information: Changes in external transmission responses 5. Review of outsourcing regulations: Addition and removal of obligations for contractors 6. Administrative fines: Narrow target range and low amounts (not worth fearing) 7. Q&A / Business card exchange

Aug 20, 2026

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[Seminar] How Will the Future of Commercial Vehicles and Related Industries Change?

  • NEW
  • SEMINAR_EVENT

[Instructor] Innovation Analyst Andy Kondo [Key Lecture Content] *The latest content will be added (changed) as appropriate based on the on-site survey of IAA Transportation 2026.* From September 15 to 20, 2026, the largest commercial vehicle exhibition in Europe, IAA Transportation, will be held in Hanover, Germany. It is a gathering place for manufacturers of commercial vehicles such as trucks and buses, as well as the parts, energy, and software that support them, occurring every two years. The cost structure of logistics, urban transportation and the environment, energy transition, decarbonization efforts, and a microcosm of the industry will reveal the future business environment just a step ahead. In this seminar, an innovation analyst who has been observing major global exhibitions such as CES and Hannover Messe for many years will report shortly after the event based on on-site coverage. Has autonomous driving become the main focus in commercial vehicles? Where is the energy transition for large vehicles settling in terms of batteries, hydrogen, and alternative fuels? How far have Chinese companies come? Based on photos taken at the venue and observations of actual products, the seminar will delve into the implications for Japanese companies.

Aug 20, 2026

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