22 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Sheath Introducer
FDA 510(k)
FDA Class 2
·Cardiovascular
ZEUS-O
FDA UDI
SPINAL ELEMENTS·00840916122492·Zeus-O Implant, 15 x 09 x 32mm
Leg Bag
FDA UDI
C. R. Bard, Inc.·00801741050909·Dispoz-A-Bag, Leg Bag with Flip-Flo Drainage Va...
Oticon
FDA UDI
Oticon A/S·05707131280398·RIA2 PRO TI, BTE 13 WL 85 CBE DEMO
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P1509320·15mm PLIF Implant 9mm Wide 32mm Length
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P15093270·15mm PLIF Implant 9mm Wide 32mm Length 7 Degrees
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869607704·TELIX K Ti Cage 9x32mm 5°
INCLUSIVE MINI IMPLANT
FDA 510(k)
FDA Class 2
·Dental
DISTAL VOLAR RADIUS ANATOMICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
RADIFOCUS OPTITORQUE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 6, 2013
ACCU-CHEK AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·September 3, 2008
AUGMENTED INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·June 29, 2011
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
NESTER PLATINUM EMBOLIZATION MICROCOIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
BD VACUTAINER® 9NC 0.109M PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 6, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018