8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
BONE MARROW NEEDLE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
POWDER FREE LATEX EXAMINATION GLOVES, BLUE, TESTED FOR USE WITH CHEMOTHERAPY DRUGS
FDA 510(k)
FDA Class 1
·General Hospital
TK Sterile Hypodermic Needle
FDA 510(k)
FDA Class 2
·General Hospital
IBALANCE TKA, MODULAR TIBIAL TRAY, SZ 5
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MBH·November 16, 2020
PS TIBIAL BEARING, SIZE 5, 10MM, VIT E
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MBH·November 16, 2020
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2014
CONCERTO II CRT-D
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code NIK·October 15, 2012
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·August 6, 2010