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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Optovue RTVue, iVue Ophthalmic Devices Optovue Inc. 2 United States USFDA
Device Recall Optical Coherence Tomography System Ophthalmic Devices Optovue, Inc. 2 United States USFDA
Device Recall Optical Coherence Tomography System Ophthalmic Devices Optovue, Inc. 2 United States USFDA
Device Recall Optical Coherence Tomography System Ophthalmic Devices Optovue, Inc. 2 United States USFDA
Device Recall Optovue iVue General and Plastic Surgery Devices Optovue Inc. 2 United States USFDA
Device Recall Optovue iVue and iVue 500 Ophthalmic Devices Optovue, Inc. 2 United States USFDA
Device Recall Cornea Power Kit (software) Ophthalmic Devices Optovue Inc. 2 United States USFDA
Device Recall Optovue iVue with Normative Database Ophthalmic Devices Optovue, Inc. 2 United States USFDA
Device Recall Optovue RTVue Optical Coherence Tomography with Normative Database Ophthalmic Devices Optovue Inc. 2 United States USFDA
iVue100 Optovue Germany BAM
iVue Optovue, Inc. Switzerland SATP