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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Low temperature sterilization systems V-PRO® 1, V-PRO® 1 Plus and V-PRO® maX Steris Corporation Spain AEMPSVFOI
Washers-Disinfectors AMSCO 3053 and 5053 STERIS SAS Spain AEMPSVFOI
AMSCO 3052 and AMSCO 5052 Single-Chamber Washer/Disinfectors equipped with an automated SCS conveyor and barcode system STERIS Corporation.. Saudi Arabia SFDA
ORT 353D, ORT 353C and ORT 01G Orthopaedic Extensions STERIS Corporation Saudi Arabia SFDA
Talon® grasping device US Endoscopy Saudi Arabia SFDA
the Surgical Lighting and Media Systems Harmony LA, LC 500 and LA 700 Steris Germany BAM
Amsco® V-Pro™1 and V-Pro™1 Plus Low Temperature Sterilization Systems Steris Germany BAM
Washer / disinfector (endoscope disinfection unit) Steris Germany BAM
V-PRO 1 / V-PRO 1 Plus / V-PRO maX Low Temperature Sterilization Systems STERIS Corporation Germany BAM
AMSCO V-PRO 1, V-PRO 1 Plus, VPRO maX Steris Corporation Germany BAM
V-PRO 60 Low Temperature Sterilization System STERIS Corporation - Monterrey Operations Germany BAM
the Velocity Biopsy Valve US Endoscopy Germany BAM
Velocity Biopsy Valve United States Endoscopy Group, Inc. Czechia MHSIDCCCDMIS
DETEX Synergy Health (UK) Ltd Czechia MHSIDCCCDMIS
Sterile maternal (obstetric) pad Synergy Health (UK) Ltd Czechia MHSIDCCCDMIS
V-PRO® 1, V-PRO® 1 Plus, and V-PRO® maX Low Temperature Sterilization Systems ITS Science & Medical Pte Ltd Singapore HSA
US Endoscopy Talon grasping device Kenda (S) Pte Ltd Singapore HSA
Talon grasping unit United States Endoscopy Group, Inc Sweden SMPA
Amsco VPRO 1 and Amsco VPRO 1 Plus Low Temperature Sterilization Systems General Hospital and Personal Use Devices Steris Corporation 2 United States USFDA
SYSTEM 1E Liquid Chemical Sterilant Processing System General Hospital and Personal Use Devices Steris Corporation 2 United States USFDA
Cmax Surgical Table General and Plastic Surgery Devices Steris Corporation 1 United States USFDA
Device Recall Reliance Vision Single Chamber Washer/Disinfector General Hospital and Personal Use Devices Steris Corporation 2 United States USFDA
Device Recall Verify SixCess Indicator Strips General Hospital and Personal Use Devices Steris Corporation 2 United States USFDA
Device Recall Verify SixCess Challenge Pack General Hospital and Personal Use Devices Steris Corporation 2 United States USFDA
Device Recall SYSTEM 1E Liquid Chemical Sterilant Processing Systm General Hospital and Personal Use Devices Steris Corporation Hopkins Facility 2 United States USFDA