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The standard DIN EN ISO 16672 applies to ocular endotamponades (OE), a group of non-solid implants used in ophthalmology to flatten and position a detached retina onto the choroid, or to tamponade the retina. With regard to the safety and efficacy of OE, this standard specifies requirements for their intended performance, design attributes, pre-clinical and clinical evaluation, sterilization, product packaging, product labelling and the information supplied by the manufacturer. The responsible German standardization committee is Working Committee is NA 027-01-20 AA "Intraokulare Medizinprodukte" ("Intraocular medical devices") at DIN Standards Committee Optics and Precision Mechanics (NAFuO).
This document replaces DIN EN ISO 16672:2003-06 .
This document has been replaced by: DIN EN ISO 16672:2022-05 .