13 results
·
27ms
·
Sources: EU EUDAMED, US FDA
OHMEDA INFANT RESUSCITATION SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
PEEK Corpectomy
FDA UDI
Nuvasive, Inc.·00887517623331·PEEK Corp Core, Ø12x43mm
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293159·
Key Surgical K-Wires and Steinmann Pins
FDA UDI
KEY SURGICAL, INC.·00849771012856·K-Wires, Single diamond, round end, .062-inch (...
NA
FDA UDI
KEY SURGICAL, INC.·10849771049477·K-Wires, Single diamond, round end, .062-inch (...
K-Wire w. lanzet/round end 1.6mm/229mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM712430·K-Wire w. lanzet/round end
1.6mm/...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484627·K-Wire w. lanzet/round end _x000D_...
Sklar
FDA UDI
SKLAR CORPORATION·10649111053559·TISS NIPPER 14MM CVX JAW 5 INCHES
METAL HEMI IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
audifon Tinnitus-Module
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
HEMOSPLIT, 14.5 FR, STANDARD KIT, 23 CM, STRAIGHT
FDA Adverse Event
Malfunction
·C. R. BARD INC. (BASD)·Product code MSD·February 1, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·January 26, 2011
LIFESTENT SOLO VASCULAR STENT SYSTEM
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·June 30, 2014