8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
SECA CHAIR SCALE-721
FDA 510(k)
FDA Class 1
·General Hospital
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR28220431·Betaflex wires Titanium Straight-Arch-F. max. ....
AMPCO SKIN SCRUB TRAYS, CAT.#SS843
FDA 510(k)SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503
FDA 510(k)
FDA Unclassified
·Unknown
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·June 23, 2023
PULSE GEN MODEL 105
FDA Adverse Event
Death
·CYBERONICS, INC.·Product code LYJ·May 20, 2014
ENDEAVOR RESOLUTE RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·November 7, 2012
3005075853-2010-04826
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·August 24, 2010