191 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DIO-DENT 10 DENTAL DIODE LASER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Battalion
FDA UDI
ALPHATEC SPINE, INC.·00840967187419·Battalion, LLIF Trial, 15°, 18 mm Wide, 19 mm X...
RADIAL HEAD IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
URINE COLLECTION, PRESERVATION AND TRANSPORT SYSTEM
FDA 510(k)
FDA Class 1
·Microbiology
DRIVING CAP BODY/FOR RADIOLUCENT INSERTION HANDLE
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code LXH·April 2, 2013
ZOOM CRITICAL CARE BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·February 25, 2011
PFC SIGMA CVD INS SZ2.5 12.5MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC., DEPUY-RAYNHAM·Product code JWH·April 17, 2008
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 16, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 11, 2010
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 23, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 9, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 18, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 16, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 2, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·October 5, 2010
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 10, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 17, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 2, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 14, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·June 6, 2011