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Withdrawn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
Current Stage
9960 - Withdrawal effective - Withdrawal
Completion Date
02-May-2018

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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
...

SLOVENSKI STANDARD
kSIST FprEN ISO 12870:2014
01-julij-2014
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: FprEN ISO 12870
ICS:
11.040.70 Oftalmološka oprema Ophthalmic equipment
kSIST FprEN ISO 12870:2014 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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

kSIST FprEN ISO 12870:2014

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

kSIST FprEN ISO 12870:2014

EUROPEAN STANDARD
FINAL DRAFT
FprEN ISO 12870
NORME EUROPÉENNE

EUROPÄISCHE NORM

April 2014
ICS 11.040.70 Will supersede 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 draft European Standard is submitted to CEN members for unique acceptance procedure. It has been drawn up by the Technical
Committee CEN/TC 170.

If this draft becomes a European Standard, 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.

This draft European Standard was established by CEN 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.

Recipients of this draft are invited to submit, with their comments, notification of any relevant patent rights of which they are aware and to
provide supporting documentation.

Warning : This document is not a European Standard. It is distributed for review and comments. It is subject to change without notice and
shall not be referred to as a European Standard.


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. FprEN ISO 12870:2014 E
worldwide for CEN national Members.

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

kSIST FprEN ISO 12870:2014
FprEN 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 ----------------------

kSIST FprEN ISO 12870:2014
FprEN 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 FprEN ISO
12870:2014 by Technical Committee CEN/TC 170 “Ophthalmic optics” the secretariat of which is held by DIN.
This document is currently submitted to the Unique Acceptance Procedure.
This document will supersede 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.
For relationship with EU Directive, see informative Annex ZA, which is an integral part of this document.
Endorsement notice
The text of ISO 12870:2012 has been approved by CEN as FprEN ISO 12870:2014 without any modification.

3

---------------------- Page: 5 ----------------------

kSIST FprEN ISO 12870:2014
FprEN ISO 12870:2014 (E)
Annex ZA
(informative)

Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC on Medical Devices
This European Standard has been prepared under a mandate given to CEN by the European Commission
and the European Free Trade Association to provide a means of conforming to Essen
...

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