5,320 results · 30ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

AORTIC CUTTER 3.8MM

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR·Product code DWS·June 13, 2011

ULTIMA OPCAB SYSTEM, STANDARD BLADE

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR·Product code DWS·June 13, 2011

2124215-2011-05734

FDA Adverse Event
Injury ·GUIDANT PUERTO RICO BV·Product code DWS·April 15, 2011

ACROBAT SUV VACUUM STABILIZER SYSTEM, ST

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DWS·April 29, 2011

ULTIMA OPCAB SYSTEM, STANDARD BLADE

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DWS·May 20, 2011

1174 PHYSIO ANNULOPLASTY RING SIZER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code DWS·September 26, 2007

ACROBAT-I POSITIONER

FDA Adverse Event
Injury ·MAQUET CARDIOVASCULAR, LLC·Product code DWS·October 21, 2014

ACROBATI-I POSITIONER

FDA Adverse Event
Injury ·MAQUET CARDIOVASCULAR, LLC·Product code DWS·October 21, 2014

ACROBAT-I

FDA Adverse Event
Injury ·MAQUET CARDIOVASCULAR, LLC·Product code DWS·October 21, 2014

ACROBAT-I POSITIONER

FDA Adverse Event
Injury ·MAQUET CARDIOVASCULAR, LLC·Product code DWS·October 21, 2014

UNKNOWN MEDTRONIC TISSUE

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code DWS·December 5, 2014

ACROBAT-I POSITIONER

FDA Adverse Event
Injury ·MAQUET CARDIOVASCULAR, LLC·Product code DWS·October 21, 2014

SCANLAN

FDA Adverse Event
Injury ·SCANLAN INTL., INC.·Product code DWS·February 17, 2005

URCHIN HEART POSITIONER

FDA Adverse Event
Malfunction ·MEDTRONIC PERFUSION SYSTEMS·Product code DWS·March 30, 2005

*

FDA Adverse Event
Other ·*·Product code DWS·February 14, 2005

MAYO-HEGAR NEEDLE HOLDERS, 8"

FDA Adverse Event
Injury ·TONTARRA·Product code DWS·January 18, 2005

DISPOSABLE PUNCH

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code DWS·July 23, 2007

HEARTPORT FORCEPS

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code DWS·July 12, 2007

1174 PHYSIO ANNULOPLASTY RING SIZER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code DWS·September 26, 2007

AORTIC PUNCH

FDA Adverse Event
Malfunction ·PORTER MEDICAL PRODUCTS, INC.·Product code DWS·July 19, 2007