849 results
·
29ms
·
Sources: EU EUDAMED, US FDA
ACUBAND ACUPRESSURE WRIST BAND DEVICE
FDA 510(k)
FDA Unclassified
·Unknown
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809843767·FOR MEN 30-40 MM HG KNEE HIGH CLOSED TOE EXTRA ...
ARx SAI
FDA UDI
Life Spine, Inc.·00190837196004·
Arx
FDA UDI
Life Spine, Inc.·00190837175528·
DBB-05 HEMODIALYSIS DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
FLEXICAST
FDA 510(k)
FDA Class 2
·Dental
1.3MM TI CRTX SCREW SLF-DRLG W/PLUSDRIVE(TM) RECESS 6MM
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code DZL·April 11, 2013
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code LDD·May 28, 2008
VIRTUOSO DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code LWS·April 13, 2011
UNKNOWN
FDA Adverse Event
Malfunction
·COOK, INC.·Product code DTK·August 21, 2014
UNK
FDA Adverse Event
Injury
·COOK, INC.·Product code DTK·August 20, 2014
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DTK·August 20, 2014
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 26, 2012
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 13, 2010
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 7, 2010
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 16, 2011
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 23, 2011
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 28, 2011
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 27, 2012
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 17, 2012