8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
n!ce for Planmill
FDA 510(k)
FDA Class 2
·Dental
ROCCIA
FDA UDI
Silony Medical GmbH·04054896028385·ROCCIA MultiLIF Cage 17x34 mm, 10° Lor.
SAVE RESUSCITATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
NEOPAP SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
PICOSURE
FDA Adverse Event
Malfunction
·CYNOSURE LLC·Product code GEX·May 3, 2024
PINN CAN BONE SCREW 6.5MMX40MM
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS ¿ REG.·Product code NDJ·October 15, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·June 17, 2013
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·July 23, 2011