33 results · 23ms · Sources: EU EUDAMED, US FDA

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CRONO AND CRONO, MODEL 30

FDA 510(k)
FDA Class 2 ·General Hospital

RABEA 0°

FDA UDI
SIGNUS Medizintechnik GmbH·04047844000427·The basic shape of the NUBIC and RABEA devices ...

RABEA 5°

FDA UDI
SIGNUS Medizintechnik GmbH·04047844000601·The basic shape of the NUBIC and RABEA devices ...

Navagio

FDA UDI
Kalitec Direct LLC·B07330K0144140·Trial, TLIF, 32L OB STR 7Deg, 14mm

POWDERED VINAL EXAM GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

KWIKKMODEL

FDA 510(k)
FDA Class 2 ·Dental

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

CHPV I-L/S W/PLAT UN120CM DIST

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·April 8, 2013

SYNCHROMED EL

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·March 24, 2011

ENDOTAK RELIANCE

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008