9 results
·
20ms
·
Sources: EU EUDAMED, US FDA
DACOMED EXTERNAL MALE CONTINENCE DEVICE
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011885323220·dentaform® Band, tooth 36, size 23/Roth 22
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011885323180·dentaform®, tooth 36, size 23/Roth 18
MEDTRONIC MODEL 5411 SURGICAL CABLE ADAPTOR
FDA 510(k)
FDA Class 2
·Cardiovascular
MODIFIED SCHNEIDER-SHILEY WIRE TORQUER
FDA 510(k)
FDA Class 2
·Cardiovascular
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 19, 2014
CE INFUSOR, LV 5 ML/H,12 PACK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·October 28, 2010
TARGET DEVICE GAMMA3 300X160MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·November 20, 2012
EQUINOXE SHOULDER COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·March 11, 2024