25 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DYNAPBV BODY SOFTWARE
FDA 510(k)
FDA Class 2
·Radiology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813827·GENUMEDI PRO SILVER SIZE II
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450392232·
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383505871·Gutta Percha Points is used to root canal filin...
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970430·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973691·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973073·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970447·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973905·
LUMINOS AGILE
FDA 510(k)
FDA Class 2
·Radiology
REPROCESSED 2515 NAV VARIABLE ELECTROPHYSIOLOGY CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·September 5, 2024
NV GXL LINER LIPPED 32MM ID, GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·September 5, 2024
ALT HA S CLR EXT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code MEH·November 14, 2023
ZEPHYR XL DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·January 13, 2014
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
ASR UNI FEMORAL IMPL SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 1, 2011
NV GXL LINER NEUTRAL, 36MM ID, GROUP 2 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·May 31, 2024
NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·August 12, 2024
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·December 2, 2015