Abstract
ISO 16672:2003 applies to ocular endotamponades (OEs), 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 OEs, ISO 16672:2003 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.
General information
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Status: WithdrawnPublication date: 2003-02Stage: Withdrawal of International Standard [95.99]
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Edition: 1Number of pages: 13
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Technical Committee :ISO/TC 172/SC 7ICS :11.040.70
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Life cycle
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Now
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Revised by
WithdrawnISO 16672:2015