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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
BD Visitec EdgeAhead MVR Knife Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Boston ES Rigid Gas Permeable Contact lens Ophthalmic Devices Bausch & Lomb Inc 2 United States USFDA
AIR OPTIX Ophthalmic Devices Ciba Vision Corporation 3 United States USFDA
Constellation Vision System Ophthalmic Devices Alcon Research LTD dba Alcon Laboratories, Inc. 2 United States USFDA
MIRA CR4050 Finger Probe Ophthalmic Devices Mira, Inc. 2 United States USFDA
MIRA CR4055 Finger Probe Ophthalmic Devices Mira, Inc. 2 United States USFDA
MIRA CR4060 Finger Probe Ophthalmic Devices Mira, Inc. 2 United States USFDA
WaveLight FS 200 Femtosecond Laser System Ophthalmic Devices Wavelight AG 1 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.00 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.01 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.02 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.10 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.15 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.16 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.18 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.20 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.21 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.22 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall STAR S4 IR Excimer Laser System; Software Version 5.30 Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall Lenstar LS 900 EyeSuite Biometry version i2.000, Ophthalmic Devices Haag-Streit USA Inc 1 United States USFDA
Device Recall Equate MutiPurpose Solution, For Soft Contact Lenses, Sterile Ophthalmic Devices Bausch & Lomb Inc 2 United States USFDA
Device Recall Bausch & Lomb Stellaris Premium Vacuum Phaco Pack, Ref: BL5110 Ophthalmic Devices Bausch & Lomb Inc 2 United States USFDA
Device Recall Bausch & Lomb Stellaris Basic Vacuum Phaco Pack, Ref: BL5111 Ophthalmic Devices Bausch & Lomb Inc 2 United States USFDA
Device Recall Bausch & Lomb Stellaris Optimized Stability Vacuum Pack, Ref: BL5112 Ophthalmic Devices Bausch & Lomb Inc 2 United States USFDA
Device Recall Bausch & Lomb Stellaris 1.8mm Premium Vacuum Phaco Pack with MICS Needle, Ref: BL5114 Ophthalmic Devices Bausch & Lomb Inc 2 United States USFDA