9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FILTERED EXTENSION SETS
FDA 510(k)
FDA Class 2
·General Hospital
INFUSOMAT SPACE PUMP IV SET
FDA Adverse Event
Malfunction
·B. BRAUN DOMINICAN REPUBLIC·Product code FPA·November 17, 2009
RAPID ONE STEP BUPRENORPHINE TEST CARD
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Sleepware G3
FDA 510(k)
FDA Class 2
·Neurology
ADAPTER SLEEVES 12/14 +2
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 5, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·December 30, 2010
530G INSULIN PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·July 17, 2014
STEALTH 32 LHOOK LAP ELEC PKG
FDA Adverse Event
Malfunction
·CONMED UTICA·Product code GEI·November 12, 2021
STEALTH 32 LHOOK LAP ELEC PKG
FDA Adverse Event
Malfunction
·CONMED UTICA·Product code GEI·November 12, 2021