9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Serranator Alto PTA Serration Balloon Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221046345·Unitek(TM) Molar Band General Purpose Wide Hard...
ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC CRYOCATH LP·Product code OAE·February 2, 2018
T:SLIM G5 SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OYC·February 12, 2020
ECHOSTIM FACET TIP
FDA 510(k)
FDA Class 2
·Anesthesiology
PROSTIVA RF THERAPY HAND PIECE PROSTIVA RF THERAPY RF GENERATOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GYNECARE TVT-AA ABDOMINAL
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·June 11, 2013
SIGMA CRVD GVF INS 2.5 10MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 8, 2011
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM, RITTER·Product code FNL·September 10, 2008