10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
LMI IRRIGATION CATHETER (IGR)
FDA 510(k)
FDA Class 2
·Cardiovascular
Lacrimal Probe
FDA UDI
KATENA PRODUCTS, INC.·00841668108840·CRAWFORD RETRIEVING HOOK
NuVasive Navigation Instruments
FDA 510(k)
FDA Class 2
·Neurology
STERILIZATION PROCESS/ABSORBENT TOWEL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SS COMPRESSION HIP SCREW LAG SCREW
FDA Adverse Event
Injury
·BIOMET TRAUMA·Product code KTT·September 19, 2016
ASSY, CONSOLE, BLADDERSCAN BVI 9400
FDA Adverse Event
Malfunction
·VERATHON MEDICAL·Product code IYO·February 15, 2013
PROPEX
FDA Adverse Event
Malfunction
·DENTSPLY MAILLEFER·Product code LQY·January 18, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·August 1, 2014
HUDSON ET TUBE, SHER-I-BRONCH, LS, 35 FR
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CBI·December 23, 2020
KATENA PRODUCTS, INC
FDA Adverse Event
Injury
·KATENA PRODUCTS, INC·Product code HNL·December 19, 2019