UL 1180 CRD-2014 UL Standard for Safety Fully Inflatable Recreational Personal Flotation Devices - Section Paragraph Reference Paragraphs 24 4 24 5 and SA6 4 2 Subject Removal of .pdf

上传人:arrownail386 文档编号:1067355 上传时间:2019-04-02 格式:PDF 页数:2 大小:12.72KB
下载 相关 举报
UL 1180 CRD-2014 UL Standard for Safety Fully Inflatable Recreational Personal Flotation Devices - Section  Paragraph Reference Paragraphs 24 4 24 5 and SA6 4 2 Subject Removal of .pdf_第1页
第1页 / 共2页
UL 1180 CRD-2014 UL Standard for Safety Fully Inflatable Recreational Personal Flotation Devices - Section  Paragraph Reference Paragraphs 24 4 24 5 and SA6 4 2 Subject Removal of .pdf_第2页
第2页 / 共2页
亲,该文档总共2页,全部预览完了,如果喜欢就下载吧!
资源描述

1、UL COPYRIGHTED MATERIAL NOT AUTHORIZED FOR FURTHER REPRODUCTION ORDISTRIBUTION WITHOUT PERMISSION FROM ULUNDERWRITERS LABORATORIES INC. CERTIFICATION REQUIREMENT DECISIONThis Certification Requirement Decision is prepared and published by Underwriters Laboratories Inc.(UL). It is normative for the a

2、pplicable UL Product Certification Program(s); however, it is currently notpart of the UL Standard(s) referenced below.Product Category (CCN): OTDGStandard Number: UL 1180Standard Title: Standard for Fully Inflatable Recreational Personal Flotation DevicesEdition Date: February 13, 2009Edition Numbe

3、r: 2Section / Paragraph Reference: Paragraphs 24.4, 24.5 and SA6.4.2Subject: Removal of Low Mark View for Type III InflatablesDECISION:24.4 In the position of relaxed face-up static balance, each test participant, after repositioning the headwhen applicable, and when looking to the side shall see th

4、e waters surface at a point within 3 m (10 ft.)from the test participants position and beyond.Exception: Type III devices are not required to comply with 24.4.24.5 In the position of relaxed face-up static balance, for all test participants, the average of the lowestmark on a vertical scale, which i

5、s placed 6 m (20 ft.) in front of the subject so that the test participant seesthe scale without moving his or her head, shall not be higher than 0.3 m (12 in.) from the water level. Forperformance Type II and III devices, test participants are able to reposition the head and the device, whenapplica

6、ble, and then relax for the measurement.Exception: Type III devices are not required to comply with 24.5.SA6.4.2 When tested as specified in UL 1180, Section 24.5 with CO2inflation, test participants are ableto reposition the head, re-adjust the device on the body and orally adjust inflation and the

7、n relax for themeasurement. After these adjustments the average lowest mark on a vertical scale shall be equal to orless than that of the average lowest mark of the hybrid-inflatable reference vest.Exception: Type III devices are not required to comply with SA6.4.2.RATIONALE FOR DECISION:The rationa

8、l for this certification requirement decision is to better align Type III inflatable devices with TypeIII inherently buoyant devices, as defined within UL 1123 and the proposed requirements within UL12402-5 regarding recreational Level 70 devices.This certification requirement decision clarifies tha

9、t the low mark requirements are not applicable to TypeIII recreational inflatable devices. Since these devices, like Type III inherently buoyant devices, areintended to be used by conscious wears in sheltered waters, the premise of the clarification is that asubject should be able to reposition thei

10、r body or head to view the waters surface when necessary.Copyright 2014 Underwriters Laboratories Inc.UL, in performing its functions in accordance with its objectives, does not guarantee or warrant thecorrectness of Certification Requirement Decisions it may issue or that they will be recognized or

11、 adoptedby anyone. Certification Requirement Decisions are the opinion of Underwriters Laboratories Inc. inUL COPYRIGHTED MATERIAL NOT AUTHORIZED FOR FURTHER REPRODUCTION ORDISTRIBUTION WITHOUT PERMISSION FROM ULpractically applying the requirements of the standard. They do not represent formal inte

12、rpretations of thestandard under American National Standards Institute (ANSI) processes. UL shall not be responsible toanyone for the use of or reliance upon Certification Requirement Decisions by anyone. UL shall not incurany obligation or liability for damages, including consequential damages, ari

13、sing out of or in connectionwith the use or reliance upon Certification Requirement Decisions. The electronic version of theCertification Requirement Decision is the current version and previously printed copies may be outdated.This document is published as a service to ULs certification customersSTANDARD NUMBER: UL 1180 -2-

展开阅读全文
相关资源
猜你喜欢
  • KS P ISO 11737-1-2012 Sterilization of medical devices-Microbiological methods-Part 1:Determination of population of microorganisms on products《医疗器械的消毒 微生物法 第1部分 产品的微生物群数的判断》.pdf KS P ISO 11737-1-2012 Sterilization of medical devices-Microbiological methods-Part 1:Determination of population of microorganisms on products《医疗器械的消毒 微生物法 第1部分 产品的微生物群数的判断》.pdf
  • KS P ISO 11953-2012 Dentistry-Implants-Clinical performance of hand torque instruments《牙科 植入 手扭矩仪器的临床性能评估》.pdf KS P ISO 11953-2012 Dentistry-Implants-Clinical performance of hand torque instruments《牙科 植入 手扭矩仪器的临床性能评估》.pdf
  • KS P ISO 11979-2-2005 Ophthalmic implants-Intraocular lenses-Part 2:Optical properties and test methods《眼科植入物 眼内晶状体 第2部分 光学特性和测试方法》.pdf KS P ISO 11979-2-2005 Ophthalmic implants-Intraocular lenses-Part 2:Optical properties and test methods《眼科植入物 眼内晶状体 第2部分 光学特性和测试方法》.pdf
  • KS P ISO 11979-6-2006 Ophthalmic implants-Intraocular lenses-Part 6:Shelf-life and transport stability 《眼科植入物 眼内晶状体 第6部分 保存期限和运输稳定性》.pdf KS P ISO 11979-6-2006 Ophthalmic implants-Intraocular lenses-Part 6:Shelf-life and transport stability 《眼科植入物 眼内晶状体 第6部分 保存期限和运输稳定性》.pdf
  • KS P ISO 11979-7-2006 Ophthalmic implants-Intraocular lenses-Part 7:Clinical investigations 《眼科植入物 眼内晶状体 第7部分 临床检测》.pdf KS P ISO 11979-7-2006 Ophthalmic implants-Intraocular lenses-Part 7:Clinical investigations 《眼科植入物 眼内晶状体 第7部分 临床检测》.pdf
  • KS P ISO 11980-2006 Ophthalmic optics-Contact lenses and contact lens care products-Guidance for clinical investigations 《眼科光学 隐形眼镜和隐形眼镜防护产品 临床检测指南》.pdf KS P ISO 11980-2006 Ophthalmic optics-Contact lenses and contact lens care products-Guidance for clinical investigations 《眼科光学 隐形眼镜和隐形眼镜防护产品 临床检测指南》.pdf
  • KS P ISO 12189-2009 Implants for surgery-Mechanical testing of implantable spinal devices-Fatigue test method for spinal implant assemblies using an anterior support《外科植入物 可植入脊骨器械的.pdf KS P ISO 12189-2009 Implants for surgery-Mechanical testing of implantable spinal devices-Fatigue test method for spinal implant assemblies using an anterior support《外科植入物 可植入脊骨器械的.pdf
  • KS P ISO 12891-2-2008 Retrieval and analysis of surgical implants-Part 2:Analysis of retrieved metallic surgical implants《外科植入物的回收与分析 第2部分 取出的金属外科植入物的分析》.pdf KS P ISO 12891-2-2008 Retrieval and analysis of surgical implants-Part 2:Analysis of retrieved metallic surgical implants《外科植入物的回收与分析 第2部分 取出的金属外科植入物的分析》.pdf
  • KS P ISO 12891-3-2008 Retrieval and analysis of surgical implants-Part 3:Analysis of retrieved polymeric surgical implants《外科植入物的回收与分析 第3部分 收回的聚合的外科植入物的分析》.pdf KS P ISO 12891-3-2008 Retrieval and analysis of surgical implants-Part 3:Analysis of retrieved polymeric surgical implants《外科植入物的回收与分析 第3部分 收回的聚合的外科植入物的分析》.pdf
  • 相关搜索

    当前位置:首页 > 标准规范 > 国际标准 > 其他

    copyright@ 2008-2019 麦多课文库(www.mydoc123.com)网站版权所有
    备案/许可证编号:苏ICP备17064731号-1