50 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ACUGLIDE BRAND ACUPUNCTURE NEEDLES
FDA 510(k)
FDA Class 2
·General Hospital
Graftmaster
FDA UDI
ABBOTT VASCULAR INC.·08717648176487·GRAFTMASTER Coronary Stent Graft System 4.50 mm...
Graftmaster
FDA UDI
ABBOTT VASCULAR INC.·08717648176494·GRAFTMASTER Coronary Stent Graft System 4.50 mm...
Graftmaster
FDA UDI
ABBOTT VASCULAR INC.·08717648176470·GRAFTMASTER Coronary Stent Graft System 4.50 mm...
DAISY FUENTES
FDA UDI
FGX INTERNATIONAL INC.·00193033427644·
DAISY FUENTES
FDA UDI
FGX INTERNATIONAL INC.·00193033427651·
DAISY FUENTES
FDA UDI
FGX INTERNATIONAL INC.·00193033427668·
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHE USA·Product code HWC·April 9, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·September 23, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·September 23, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·October 7, 2015
TUNA (TRANS URETHRA NEEDLE) OFFICE SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AMBU GEL, HYDROGEL BURN DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·June 16, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·November 13, 2014
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES SELZACH·Product code HWC·June 2, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 5, 2016
CADD EXTENSION
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FPA·October 22, 2024
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·July 30, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·February 15, 2017