17 results
·
27ms
·
Sources: EU EUDAMED, US FDA
INORGANIC PHOSPHORUS REAGENT SET
FDA 510(k)
FDA Class 1
·Clinical Chemistry
FIXATE TISSUE BAND
FDA 510(k)
FDA Class 2
·Neurology
SYNERGY FLOW
FDA 510(k)
FDA Class 2
·Dental
UniTip Catheter
FDA UDI
Unisensor AG·07640172972113·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971604·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971611·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973585·
UniTip Catheter
FDA UDI
Unisensor AG·07640172972106·
M2A-38 CUP NON FLARED SZ 60MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2014
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC MILACA, INC.·Product code LWP·October 31, 2012
RSVR MMT-332A 10PK PRDGM 3CC 14L
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code FMF·August 20, 2010
OXF ANAT BRG LT MD SIZE 4 PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·September 28, 2022
OXF UNI TIB TRAY SZ B LM PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·September 28, 2022
8015 ALARIS SYSTEM PC UNIT
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·December 21, 2020
ORTHOPEDIC SALVAGE SYSTEM COMPRESS SEGMENTAL FEMORAL COMPONENT LEFT 8.5CM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·March 4, 2019
CPS XS SHT SPDL W PINS 600LBF
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 23, 2019
CPS CENTERING SLEEVE 21MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 23, 2019