10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
BLOOD PRESSURE MONITORING DEVICES
FDA 510(k)
FDA Class 2
·Cardiovascular
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113805·PS-C Insert, Size 6 x 14mm
Legacy
FDA UDI
Gc Orthodontics America Inc.·E53582261400001·LEGACY 1. MOLAR UPR LFT SZ 14
UniTip Catheter
FDA UDI
Unisensor AG·07640172972342·
INVIGRA
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
VINTAGE MP PRESS OVER
FDA 510(k)
FDA Class 2
·Dental
OT VERIO SYNC METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2014
HOMECHOICE
FDA Adverse Event
Death
·BAXTER HEALTHCARE - LARGO·Product code FKX·November 7, 2012
SYNCRHOMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·August 27, 2010
Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018