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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Cypass R system implant to decrease the Cypass pressure Ophthalmic Devices N/A Colombia INVIMA
cypass system 241 Ophthalmic Devices ALCON LABORATORIES Italy MSHM
CyPass® Micro-Stent Ophthalmic Devices Alcon France ANSM
COMPLETE® MoisturePLUS Ophthalmic Devices AMO France ANSM
Device Recall Ziemer Femto LDV ZGeneration Femtosecond Surgical Lasers Ophthalmic Devices Ziemer Usa Inc 2 United States USFDA
Device Recall VisiPlugST or CollaSyn Plugs Ophthalmic Devices Lacrimedics Inc Unclassified United States USFDA
Device Recall MC500 Multicolor Laser Photocoagulator Ophthalmic Devices Nidek Inc 2 United States USFDA
Device Recall ML7090 Microkeratome Blade Ophthalmic Devices Med-logics Inc 1 United States USFDA
Device Recall FORUM Archive and Viewer Ophthalmic Devices Carl Zeiss Meditec AG 2 United States USFDA
Device Recall YC1800 OPHTHALMIC YAG LASER SYSTEM Ophthalmic Devices Nidek Inc 2 United States USFDA
Device Recall LIS27T Lacrimal Intubation Set Ophthalmic Devices Quest Medical, Inc. 1 United States USFDA
Device Recall Catalys Precision Laser System Ophthalmic Devices Optimedica Corporation 2 United States USFDA
Device Recall Steriseal BiManual Irrigating/Aspirating Handpiece Ophthalmic Devices Hill-Rom, Inc. 1 United States USFDA
Device Recall OptiMedica Catalys Precision Laser System Ophthalmic Devices Abbott Medical Optics, Inc. 2 United States USFDA
Device Recall Volk 25D Large Clear BIO Lens with case UPC: 8 11608 01010 6. Ophthalmic Devices Volk Optical Inc 2 United States USFDA
Device Recall Lombart 90D Clear with case Ophthalmic Devices Volk Optical Inc 1 United States USFDA
Device Recall EC5000 Excimer Laser Corneal Surgery System Ophthalmic Devices Nidek Inc 3 United States USFDA
Device Recall Alcon Accurus Standalone Vitreous Probe Paks Ophthalmic Devices Alcon Research, Ltd. 2 United States USFDA
Device Recall OPDScan III Refractive Power/Corneal Analyzer Opthalmic Ophthalmic Devices Nidek Inc 1 United States USFDA
Device Recall RETINA PACK Ophthalmic Devices Customed, Inc 2 United States USFDA
Device Recall OPHTHALMIC PACK Ophthalmic Devices Customed, Inc 2 United States USFDA
Device Recall OPHTHALMIC PACK Ophthalmic Devices Customed, Inc 2 United States USFDA
Device Recall CATARACT PACK Ophthalmic Devices Customed, Inc 2 United States USFDA
Device Recall Customed Ophthalmic Devices Customed, Inc 2 United States USFDA
Device Recall Customed Ophthalmic Devices Customed, Inc 2 United States USFDA