DIN EN ISO 16672:2022-05
Ophthalmic implants - Ocular endotamponades (ISO 16672:2020); German version EN ISO 16672:2021
| Fecha edición: |
2022-05-01
En Vigor
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|---|---|
| Idiomas disponibles: | Inglés, Alemán |
| Resumen: | Specification of requirements for the intended performance, design attributes, pre-clinical and clinical evaluation, sterilisation, product packaging, product labelling and the information to be supplied by the manufacturer for endotamponades used in ocular surgery. |
| Keywords: | Clinical investigations|Clinical testing|Data of the manufacturer|Definitions|Design|Durability|Endotamponades|Evaluations|Implants (surgical)|Investigation condition|Investigations|Marking|Medical devices|Medical products|Oculars|Ophthalmic equipment|Ophthalmic optics|Ophthalmology|Optics|Packages|Properties|Retina|Safety|Specification (approval)|Sterilization (hygiene)|Storage quality|Surgery|Surgical implants|Tamponade|Testing|Transport |
| ICS: | 11.040.70 - Equipo oftálmico |
| CTN: | |
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Equivalencia Internacional |
Idéntica EN ISO 16672:2021 Idéntica ISO 16672:2020 |
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Reemplazo Normas |
Reemplaza a DIN EN ISO 16672:2015-12 Reemplaza a DIN EN ISO 16672:2018-08 |










