EN ISO 11979-10This description is for standard: EN ISO 11979-10ISO 11979-10:2006 is applicable to any intraocular lens (IOL) whose primary indication is the modification of the refractive power of a
EN ISO 11979-3This description is for standard: EN ISO 11979-3ISO 11979-3:2006 specifies requirements and test methods for certain mechanical properties of intraocular lenses (IOLs). It is applicab
EN ISO 11979-4This description is for standard: EN ISO 11979-4ISO 11979-4:2008 specifies the labelling requirements for intraocular lenses (IOLs) and the information to be provided within or on the pa
EN ISO 11979-5This description is for standard: EN ISO 11979-5ISO 11979-5:2006 specifies particular requirements for the biocompatibility evaluation of materials for intraocular lenses (IOLs) includin
EN ISO 11979-6This description is for standard: EN ISO 11979-6ISO 11979-6:2007 specifies tests by which the shelf-life of sterile intraocular lenses (IOLs) in their final packaging can be determined.
EN ISO 11979-7This description is for standard: EN ISO 11979-7ISO 11979-7:2006 specifies particular requirements for clinical investigations for posterior and anterior chamber monofocal intraocular le
EN ISO 11979-8This description is for standard: EN ISO 11979-811979-8:2006 specifies fundamental requirements for all types of intraocular lenses intended for surgical implantation into the anterior s
EN ISO 11979-9This description is for standard: EN ISO 11979-9ISO 11979-9:2006 is applicable to any intraocular lens whose optic provides two or more rotationally symmetric powers and whose primary in
EN ISO 15798This description is for standard: EN ISO 15798ISO 15798:2010 is applicable to ophthalmic viscosurgical devices (OVDs), a class of non-active surgical implants with viscous and/or viscoelas