33 results
·
39ms
·
Sources: EU EUDAMED, US FDA
ESPRIT VENTILATOR WITH NICO-ESPRIT INTERFACE OPTION, MODEL V1000
FDA 510(k)
FDA Class 2
·Anesthesiology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756772402·Esophageal Stethoscope w/Temperature Sensor
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0144120·Trial, TLIF, 32L OB STR 7Deg, 12mm
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981177058·Steep DTS Guide, 12mm
K041492
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 18, 2021
POWDER-FREE VINYL EXAM GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
PM 1800 CONSERVING DEVICE
FDA 510(k)
FDA Class 2
·Anesthesiology
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Death
·MEDTRONIC XOMED INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Death
·MEDTRONIC XOMED, INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code EQJ·August 5, 2014
TRICUT® ANGLE-TIP BRONCHIAL BLADE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code EQJ·August 5, 2014
HAKIM INLINE PROGRAMMABLE VALVE SG
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code JXG·April 8, 2013
VITALITY VR
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008