EN ISO 11979-7:2014
(Main)Ophthalmic implants - Intraocular lenses - Part 7: Clinical investigations (ISO 11979-7:2014)
Ophthalmic implants - Intraocular lenses - Part 7: Clinical investigations (ISO 11979-7:2014)
ISO 11979-7:2014 specifies particular requirements for clinical investigations for posterior and anterior chamber intraocular lenses (IOLs).
Ophthalmische Implantate - Intraokularlinsen - Teil 7: Klinische Prüfungen (ISO 11979-7:2014)
Dieser Teil von ISO 11979 legt besondere Anforderungen an die klinische Prüfung von Hinterkammer- und Vorderkammer-Intraokularlinsen (IOLs) fest.
Implants ophtalmiques - Lentilles intraoculaires - Partie 7: Investigations cliniques (ISO 11979-7:2014)
L'ISO 11979-7:2014 spécifie les exigences particulières relatives aux investigations cliniques sur les lentilles intraoculaires (LIO) de chambres antérieure et postérieure.
Očesni vsadki (implantati) - Intraokularne leče - 7. del: Klinične raziskave (ISO 11979-7:2014)
Standard ISO 11979-7 določa posebne zahteve za klinične raziskave za intraokularne leče v zadnjem in sprednjem prekatu.
General Information
Relations
Standards Content (Sample)
SLOVENSKI STANDARD
SIST EN ISO 11979-7:2014
01-november-2014
1DGRPHãþD
SIST EN ISO 11979-7:2006
SIST EN ISO 11979-7:2006/A1:2012
2þHVQLYVDGNL LPSODQWDWL ,QWUDRNXODUQHOHþHGHO .OLQLþQHUD]LVNDYH ,62
Ophthalmic implants - Intraocular lenses - Part 7: Clinical investigations (ISO 11979-
7:2014)
Ophthalmische Implantate – Intraokularlinsen - Teil 7: Klinische Prüfungen (ISO 11979-
7:2014)
Implants ophtalmiques - Lentilles intraoculaires - Partie 7: Investigations cliniques (ISO
11979-7:2014)
Ta slovenski standard je istoveten z: EN ISO 11979-7:2014
ICS:
11.040.70 Oftalmološka oprema Ophthalmic equipment
SIST EN ISO 11979-7:2014 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN ISO 11979-7:2014
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SIST EN ISO 11979-7:2014
EUROPEAN STANDARD
EN ISO 11979-7
NORME EUROPÉENNE
EUROPÄISCHE NORM
September 2014
ICS 11.040.70 Supersedes EN ISO 11979-7:2006
English Version
Ophthalmic implants - Intraocular lenses - Part 7: Clinical
investigations (ISO 11979-7:2014)
Implants ophtalmiques - Lentilles intraoculaires - Partie 7: Ophthalmische Implantate - Intraokularlinsen - Teil 7:
Investigations cliniques (ISO 11979-7:2014) Klinische Prüfungen (ISO 11979-7:2014)
This European Standard was approved by CEN on 18 July 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 11979-7:2014 E
worldwide for CEN national Members.
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SIST EN ISO 11979-7:2014
EN ISO 11979-7:2014 (E)
Contents Page
Foreword .3
2
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SIST EN ISO 11979-7:2014
EN ISO 11979-7:2014 (E)
Foreword
This document (EN ISO 11979-7:2014) has been prepared by Technical Committee ISO/TC 172 “Optics and
photonics” in collaboration with 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 March 2015, and conflicting national standards shall be withdrawn at
the latest by March 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 11979-7:2006.
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
The text of ISO 11979-7:2014 has been approved by CEN as EN ISO 11979-7:2014 without any modification.
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SIST EN ISO 11979-7:2014
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SIST EN ISO 11979-7:2014
INTERNATIONAL ISO
STANDARD 11979-7
Third edition
2014-09-01
Ophthalmic implants — Intraocular
lenses —
Part 7:
Clinical investigations
Implants oph
...
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