美洲

其他

圖樣週圍的字義解釋: 其中
E134780 代表 ： UL 給致伸產品所使用的專屬檔案編號，如為不同的產品類別(如延長線則為E200250)，則UL會編排新的檔案編號給我們認證申請使用；當然個別的
客戶則有自己的專屬檔案代號，若客人需我們代為向UL申請時，則須提供授權信我們才可以代為申請。
2G55 代表目錄 ： UL 編給我們公司的產品UL內部文件控制代碼。
I.T.E. ACCESSORY 代表： "資訊產品類" 的標注說明，不可省略，報告上已有控制必須要標示。

規定 Annual report 美國食品藥物管理法: 廠商自行按照FDA規定每年9月報備年報(郵戳為準是FDA窗口收到報告的時間為準)，核報所有的販售美國的機種與數量
大部分的FDA要求可以與60825-1合併標示，但只有
Complies with 21 CFR 1040.10 and 1040.11 except for deviations pursuant to Laser Notice No. 50, dated June 24, 2007 這句不可以，需要外加上去。

手冊 (需要全文完整放置)
Complies with FDA performance standards for laser products except for deviations pursuant to Laser Notice No. 50, dated June 24, 2007.
或 Complies with 21 CFR 1040.10 and 1040.11 except for deviations pursuant to Laser Notice No. 50, dated June 24, 2007.
出處 Laser Products - Conformance with IEC 60825-1 and IEC 60601-2-22; (Laser Notice No. 50)
Document issued on: June 24, 2007
This document supersedes Laser Products – Conformance with IEC 60825-1, Am. 2 and IEC 60601-2-22; Final Guidance for Industry and FDA (Laser Notice No. 50), July 26, 2001.

What should manufacturers do in using this guidance?
Use the following modified statement of compliance on the certification label: “Complies with FDA performance standards for laser products except for deviations pursuant to Laser Notice No. 50, dated (Insert date of this guidance.)” or “Complies with 21 CFR 1040.10 and 1040.11 except for deviations pursuant to Laser Notice No. 50, dated June 24, 2007”; and Submit product reports or supplemental reports to describe changes to products in accordance with this guidance

出處 IEC 60825-1 要求標示內容如下 6.1:
For laser radiation levels above the AEL of Class 1, a description of any radiation pattern(s) emitted from the protective housing during the performance of operation and maintenance procedures. Where applicable, this shall include a statement in appropriate units of:
** wavelength,
** beam divergence,
** pulse duration and repetition rate (or description of irregular pulse pattern),
** maximum power or energy output.