23 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LigaSure Exact Dissector, Nano-coated
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CENTRONAIL TITANIUM UNIVERSAL FEMORAL NAILING SYSTEM
FDA UDI
ORTHOFIX SRL·18054242511427·GUIDE WIRE WITH OLIVE D. 3X980 MM
Centronail Titanium Universal Femoral Nailing System
FDA UDI
ORTHOFIX SRL·18032937169184·GUIDE WIRE WITH OLIVE D.3X980 MM STERILE
CAIS STAPLE
FDA 510(k)
FDA Class 2
·Orthopedic
MRI SYTEMS
FDA 510(k)
FDA Class 2
·Radiology
OPTICROSS HD
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·March 28, 2025
OPTICROSS? HD
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·July 7, 2025
OPTICROSS? HD
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·July 22, 2025
OPTICROSS? HD
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·February 11, 2025
OPTICROSS? HD
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·April 3, 2025
OPTICROSS? HD
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·December 11, 2025
OPTICROSS? HD
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·September 16, 2025
MPACT DOUBLE MOBILITY HC LINER 28/DME
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MEH·May 8, 2018
OPTICROSS? HD
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·January 13, 2026
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·June 7, 2013
ALTRUA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 23, 2011
GIRAFFE OMNIBED
FDA Adverse Event
Malfunction
·OHMEDA MEDICAL·Product code FMZ·September 29, 2014
FlowGate2 8F x 85cm, Catalog: 90485 FlowGate2 8F x 95cm, Catalog: 90495
FDA Enforcement
Class II
·Ongoing·Stryker Neurovascular·June 5, 2024
OPTICROSS? HD
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·May 22, 2025
BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQO·January 18, 2019