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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall OASIS Medical Vidaurri LASIK Flap Irrigator Ophthalmic Devices Oasis Medical Inc 1 United States USFDA
Device Recall OASIS Medical Vidaurri LASIK Flap Irrigator Ophthalmic Devices Oasis Medical Inc 1 United States USFDA
Device Recall OASIS Medical Vidaurri LASIK Flap Irrigator Ophthalmic Devices Oasis Medical Inc 1 United States USFDA
Device Recall OASIS Medical Vidaurri LASIK Flap Irrigator Ophthalmic Devices Oasis Medical Inc 1 United States USFDA
Device Recall BD Ophthalmic Ophthalmic Devices BD Opthalmic Systems 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall Alcon Trocar Cannula Replacement Plug Ophthalmic Devices Alcon Research, Ltd 1 United States USFDA
Device Recall CustomPak Surgical Packs Ophthalmic Devices Alcon Laboratories, Inc 1 United States USFDA
Device Recall CustomPak Surgical Packs Ophthalmic Devices Alcon Laboratories, Inc 1 United States USFDA
Device Recall CustomPak Surgical Packs Ophthalmic Devices Alcon Laboratories, Inc 1 United States USFDA
Device Recall CustomPak Surgical Packs Ophthalmic Devices Alcon Laboratories, Inc 1 United States USFDA
Device Recall CustomPak Surgical Packs Ophthalmic Devices Alcon Laboratories, Inc 1 United States USFDA