60 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ETEST Plazomicin (PLZ) (0.016-256 µg/mL)
FDA 510(k)
FDA Class 2
·Microbiology
ReLine
FDA UDI
Nuvasive, Inc.·00195377047519·RELINE-O Trial, 8mm H Offset Right L-pop
Pantheon System
FDA UDI
ADLER ORTHO SPA·08050880237692·Pantheon Salvage Cementless Stem L 115 Ø 12
PED. VHS VARI-ANGLE HIP SCREW
FDA UDI
Biomet Orthopedics, LLC·00880304279681·
Zavation
FDA UDI
Zavation LLC·00842166131682·Ti3Z CIF 12mmx14mmx12mm -5 deg
METZENBAUM SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896055209·METZENBAUM SCISSORS DELICATE CURVED TUNGSTEN CA...
My Medical
FDA UDI
My Medical Store LLC·G4252005120·Rhinoplasty Rasp, Curved
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306805561·Preservation Rhinoplasty: 3mm Rasp, Curved
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361021391·A-CIFT SoloFuse 4.2 Screw, Lag, 12mm
CADD® CADD®-SOLIS VIP AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FRN·November 1, 2018
OSCILLOMITT, MODELS CM 1050, CM 1040, CM 1030, CM 1020, CM 1010
FDA 510(k)
FDA Class 2
·Cardiovascular
MTI ST#1 SILICONE PESSARY
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CADD-SOLIS VIP AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FRN·June 6, 2019
CADD SOLIS VIP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC·Product code FRN·March 8, 2020
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·January 13, 2006
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·December 16, 2020
CADD-SOLIS VIP AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FRN·August 23, 2022
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETES CARE·Product code LZG·August 5, 2016
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·November 22, 2019
MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAN·November 22, 2019