36 results · 20ms · Sources: EU EUDAMED, US FDA

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TRAXIS CEMENT RESTRICTOR

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

CPAP SYSTEM, MODEL 102001

FDA 510(k)
FDA Class 2 ·Anesthesiology

VENODYNE DVT ADVANTAGE PLUS

FDA 510(k)
FDA Class 2 ·Cardiovascular

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SENSOR MODULE FOR BUBBLE DETECTOR

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTW·October 21, 2016

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·April 2, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·March 16, 2011

MARYLAND BIPOLAR FORCEPS INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC.·Product code GEI·April 18, 2008

LCD TOUCHSCREEN, RP150, S5

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 14, 2012

LCD TOUCHSCREEN, RP150, S5

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 15, 2012

S5 SINGLE ROLLER PUMP

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·April 21, 2010

S5 ROLLER PUMP

FDA Adverse Event
Malfunction ·Product code DTQ·April 11, 2011