16 results
·
21ms
·
Sources: EU EUDAMED, US FDA
DIGIARC 100AU+
FDA 510(k)
FDA Class 2
·Radiology
UniTip Catheter
FDA UDI
Unisensor AG·07640172973868·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973783·
MAX ORIENT SUCTION DEVICE FOR ELECTROCAUTERIZER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AFT PROXIMAL HUMERUS FRACTURE PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
8CH INFINITY DBS LEAD KIT, 40CM, 0.5, B
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code MHY·June 17, 2024
INTIMA-II Y 24GAX0.75IN PRN EC SLM NPVC
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FMF·April 6, 2020
BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·February 26, 2020
BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·December 3, 2019
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 4, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·June 27, 2011
BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·January 3, 2020
HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP
FDA Adverse Event
Death
·HEARTWARE, INC.·Product code DSQ·October 27, 2025
HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP
FDA Adverse Event
Injury
·HEARTWARE, INC.·Product code DSQ·October 27, 2025
BD INTIMA-II CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·July 31, 2020