20 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer
FDA 510(k)
FDA Class 2
·Cardiovascular
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970584·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970126·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970591·
ARP RX100
FDA 510(k)
FDA Class 2
·Physical Medicine
NOTOUCH BREASTSCAN
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
NEXTAR INFRARED CAMERA
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·September 10, 2021
OMNIPOD 5 POD
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code QFG·February 13, 2023
OMNIPOD 5 POD
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code QFG·February 13, 2023
OMNIPOD 5 POD
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code QFG·February 13, 2023
SEGURA HEMISPHERE STONE RETRIEVAL BASKET
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code FFL·October 7, 2008
MICRO-MATE TURBERCULIN GLASS SYRINGE
FDA Adverse Event
Malfunction
·CADENCE INC.·Product code DWO·June 25, 2013
HIP DRILLS & GUIDES
FDA Adverse Event
Malfunction
·SMITH & NEPHEW ENDOSCOPY·Product code NBH·August 5, 2011
DURAL ALPHA INSERT W RIM II/32
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LPH·March 12, 2019
DURASUL, ALPHA INSERT, HOODED, II/32
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LPH·September 28, 2018
METASUL, ALPHA INSERT, JJ/28
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·February 4, 2019
DURASUL, ALPHA INSERT, KK/36
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·March 13, 2018
COCR HEAD 32/ 0 'M' 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·June 4, 2019
DURASUL, ALPHA INSERT, LL/36
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·April 29, 2019
DURASUL, ALPHA INSERT, HOODED, KK/32
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LPH·June 15, 2018