BS DD ENV 13759-2001
家具.座椅.活动沙发床斜靠和/或微倾机构以及操作机构的耐用性能测定的试验方法已作废

Domestic furniture - Seating - Test method for the determination of the durability of reclining and/or tilting mechanisms and operating mechanisms for convertible sofa beds

BS DD ENV 13759-2001 发布历史

This ENV specifies a test method foe the determination of the durability of hand and power operated reclining and tilting mechanisms. It also specifies test methods for the determination of durability of mechanisms for cinverting sofas and chairs into beds. Test methods for strength and durability of the structure are not included, for which references shall be made to prEN 1728:1998 and to EN 1725. It does not apply to testing electrical components except for their function as part of the mechanism under test nor does if apply to seating which comes within the scope of the medical device directive.

BS DD ENV 13759-2001由英国标准学会 GB-BSI 发布于 2001-02-15，并于 2001-02-15 实施，于 2012-11-30 废止。

BS DD ENV 13759-2001 在中国标准分类中归属于: Y81 家具制品，在国际标准分类中归属于: 97.140 家具。

BS DD ENV 13759-2001的历代版本如下：

• 2001年02月15日 BS DD ENV 13759-2001 家具.座椅.活动沙发床斜靠和/或微倾机构以及操作机构的耐用性能测定的试验方法

BS DD ENV 13759-2001 家具.座椅.活动沙发床斜靠和/或微倾机构以及操作机构的耐用性能测定的试验方法 于 2012-11-30 变更为 BS EN 13759-2012 家具.座椅和沙发床的操作机构.试验方法。

非常抱歉，我们暂时无法提供预览，您可以试试： 免费下载 BS DD ENV 13759-2001 前三页，或者稍后再访问。

注意： 点击下载后，生成下载文件时间比较长，请耐心等待......

标准号

BS DD ENV 13759-2001

发布日期

2001年02月15日

实施日期

2001年02月15日

废止日期

2012-11-30

中国标准分类号

Y81

国际标准分类号

97.140

发布单位

GB-BSI

代替标准

BS EN 13759-2012

适用范围

This ENV specifies a test method foe the determination of the durability of hand and power operated reclining and tilting mechanisms. It also specifies test methods for the determination of durability of mechanisms for cinverting sofas and chairs into beds. Test methods for strength and durability of the structure are not included, for which references shall be made to prEN 1728:1998 and to EN 1725. It does not apply to testing electrical components except for their function as part of the mechanism under test nor does if apply to seating which comes within the scope of the medical device directive.