33 results · 39ms · Sources: EU EUDAMED, US FDA

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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