SS-EN-ISO-12870 Ophthalmic optics - Spectacle frames - Requirements and test methods (ISO 12870:2016)

SS-EN-ISO-12870 - 2018 EDITION - CURRENT
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ISO 12870:2016 specifies fundamental requirements for unglazed spectacle frames designed for use with all prescription lenses. It is applicable to frames at the point of sale by the manufacturer or supplier to the retailer. This International Standard is applicable to all spectacle frame types, including rimless mounts, semi-rimless mounts and folding spectacle frames. It is also applicable to spectacle frames made from natural organic materials. NOTE See Annex A for recommendations on the design of spectacle frames. ISO 12870:2016 is not applicable to complete custom-made spectacle frames or to products designed specifically to provide personal eye protection.

To find similar documents by classification:

11.040.70 (Ophthalmic equipment Including ophthalmic implants, glasses, contact lenses and their cleaning products)


Medical devices. Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market

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Designation Name

SS-EN ISO 12870:2018

Revision Level

2018 EDITION

Status

Current

Publication Date

May 7, 2018

Language(s)

English

Page Count

48

International Equivalent

EN ISO 12870:2018(IDT); ISO 12870:2016(IDT)