EN ISO 12870:2014

Ophthalmic optics - Spectacle frames - Requirements and test methods (ISO 12870:2012)

Revision of EN ISO 12870:2012, taking over ISO 12870:2012 (unchanged), in order to revise its European Annex ZA.

Augenoptik - Brillenfassungen - Anforderungen und Prüfverfahren (ISO 12870:2012)

Diese Internationale Norm legt grundlegende Anforderungen für unverglaste Brillenfassungen fest, die zur Verwendung mit allen Korrektionsgläsern bestimmt sind. Sie ist zum Zeitpunkt des Verkaufs der Brillen-fassung durch den Hersteller oder Lieferant an den Wiederverkäufer gültig.
Diese Internationale Norm gilt für alle Brillenfassungsarten, einschließlich randloser, halb-randloser und zusammenklappbarer Brillenfassungen. Sie gilt auch für Brillenfassungen aus natürlichen organischen Materialien.
ANMERKUNG   Empfehlungen bezüglich der Konstruktion von Brillenfassungen siehe Anhang A.
Diese Internationale Norm gilt nicht für als Sonderanfertigung hergestellte Brillenfassungen und für Produkte, die speziell für den persönlichen Augenschutz bestimmt sind.

Optique ophtalmique - Montures de lunettes - Exigences et méthodes d'essai (ISO 12870:2012)

Očesna optika - Okviri očal - Zahteve in preskusne metode (ISO 12870:2012)

General Information

• Status: Withdrawn
• Publication Date: 14-Oct-2014
• Withdrawal Date: 01-May-2018
• ICS: 11.040.70 - Ophthalmic equipment
• Technical Committee: CEN/TC 170 - Ophthalmic optics
• Drafting Committee: CEN/TC 170 - Ophthalmic optics
• Current Stage: 9960 - Withdrawal effective - Withdrawal
• Completion Date: 02-May-2018
• Directive: 2007/47/EC - 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
• Directive: 93/38/EEC - Procurement procedures of entities operating in the water, energy, transport and telecommunications sectors
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Mandate: M/023 - Standardization mandate to CEN/CENELEC concerning the development of European standards relating to medical devices
• Ref Project: SIST EN ISO 12870:2015 - Ophthalmic optics - Spectacle frames - Requirements and test methods (ISO 12870:2012)

Relations

• Replaces: EN ISO 12870:2012 - Ophthalmic optics - Spectacle frames - Requirements and test methods (ISO 12870:2012)
• Effective Date: 08-Jun-2022
• Replaced By: EN ISO 12870:2018 - Ophthalmic optics - Spectacle frames - Requirements and test methods (ISO 12870:2016)
• Effective Date: 09-May-2018

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 12870:2015
01-januar-2015
1DGRPHãþD
SIST EN ISO 12870:2012
2þHVQDRSWLND2NYLULRþDO=DKWHYHLQSUHVNXVQHPHWRGH,62
Ophthalmic optics - Spectacle frames - Requirements and test methods (ISO
12870:2012)
Augenoptik - Brillenfassungen - Anforderungen und Prüfverfahren (ISO 12870:2012)
Optique ophtalmique - Montures de lunettes - Exigences et méthodes d'essai (ISO
12870:2012)
Ta slovenski standard je istoveten z: EN ISO 12870:2014
ICS:
11.040.70 Oftalmološka oprema Ophthalmic equipment
SIST EN ISO 12870:2015 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------

SIST EN ISO 12870:2015

---------------------- Page: 2 ----------------------

SIST EN ISO 12870:2015

EUROPEAN STANDARD
EN ISO 12870

NORME EUROPÉENNE

EUROPÄISCHE NORM
October 2014
ICS 11.040.70 Supersedes EN ISO 12870:2012
English Version
Ophthalmic optics - Spectacle frames - Requirements and test
methods (ISO 12870:2012)
Optique ophtalmique - Montures de lunettes - Exigences et Augenoptik - Brillenfassungen - Anforderungen und
méthodes d'essai (ISO 12870:2012) Prüfverfahren (ISO 12870:2012)
This European Standard was approved by CEN on 3 October 2014.

CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European
Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national
standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member.

This European Standard exists in three official versions (English, French, German). A version in any other language made by translation
under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same
status as the official versions.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania,
Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United
Kingdom.





EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2014 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 12870:2014 E
worldwide for CEN national Members.

---------------------- Page: 3 ----------------------

SIST EN ISO 12870:2015
EN ISO 12870:2014 (E)
Contents Page
Foreword .3
Annex ZA (informative) Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC on Medical Devices .4

2

---------------------- Page: 4 ----------------------

SIST EN ISO 12870:2015
EN ISO 12870:2014 (E)
Foreword
The text of ISO 12870:2012 has been prepared by Technical Committee ISO/TC 172 “Optics and photonics”
of the International Organization for Standardization (ISO) and has been taken over as EN ISO 12870:2014 by
Technical Committee CEN/TC 170 “Ophthalmic optics” the secretariat of which is held by DIN.
This European Standard shall be given the status of a national standard, either by publication of an identical
text or by endorsement, at the latest by April 2015, and conflicting national standards shall be withdrawn at the
latest by April 2015.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN ISO 12870:2012.
This document has been prepared under a mandate given to CEN by the European Commission and the
European Free Trade Association, and supports essential requirements of EU Directive(s).
For relationship with EU Directive(s), see informative Annex ZA, which is an integral part of this document.
According to the CEN-CENELEC Internal Regulations, the national standards organizations of the following
countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech
Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece,
Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal,
Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom.
Endorsement notice
...