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

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MODIFICATION TO CD HORIZON SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Entuit Thrive

FDA UDI
XERIDIEM MEDICAL DEVICES, INC.·00827002356177·Entuit Gastrostomy BR Balloon Retention Feeding...

MODIFICATION TO LIPOPROTEIN (A) SPQ III ANTIBODY REAGENT SET

FDA 510(k)
FDA Class 2 ·Immunology

NORMED EXTREMITY TITANIUM HAND AND SMALL FRAGMENT SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

TELIGEN

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 8, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 23, 2011

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
JUMAO - JM - E. CHINA·Product code IOR·August 27, 2014

OT ULTRAMINI

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 1, 2010

OT ULTRA EASY METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 3, 2012

OT ULTRAMINI

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 7, 2010

OT ULTRA EASY METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 14, 2012

OT ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·June 3, 2011

OT ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·May 2, 2011

OT ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·May 11, 2011

OT ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 20, 2012

OT ULTRAMINI

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·November 23, 2010

OT ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·July 5, 2011

OT ULTRAMINI

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 6, 2011

OT ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·May 27, 2011

OT ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 31, 2012