9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SurgiMend MP Collagen Matrix for Soft Tissue Reconstruction
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304254718·
NI
FDA Adverse Event
Injury
·DEXCOM, INC.·Product code MDS·December 27, 2018
CHLORINATED, POLYMER-COATED POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM
FDA 510(k)
FDA Class 1
·General Hospital
CELOX TRAUMA GAUZE AG, CELOX HEMOSTATIC ANTIBACTERIAL TRAUMA GAUZE, OMNI-STAT TRAUMA GAUZE AG, OMNI-STAT HEMOSTATIC ANTI
FDA 510(k)
FDA Unclassified
·Unknown
BD VACUTAINER® WINGED SAFETY PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·December 5, 2017
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 11, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·July 15, 2011
ULTRASITE OUTLOOK SAFETY INFUSION SYSTEM IV SET
FDA Adverse Event
Malfunction
·B.BRAUN MEDICAL, INC.·Product code FPA·September 11, 2008