29 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NEXSTAT (TM) TOPICAL HEMOSTAT POWDER; NEXFOAM (R) TOPICAL SPONGE
FDA 510(k)
FDA Unclassified
·Unknown
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973257·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973301·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970041·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970065·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970058·
EZout
FDA UDI
STRYKER CORPORATION·07613327129427·Insert Tray
Raw Surgical Corporation
FDA UDI
RAW SURGICAL CORPORATION·G508RSC1024590·Operating Scissors, Straight, blunt-blunt point...
MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH
FDA 510(k)
FDA Class 2
·Cardiovascular
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970010·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970027·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172974018·UniTip High Resolution Catheter 10F
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 2, 2019
INTELLIVUE INFO CENTER IX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MHX·December 19, 2023
EMPTY CONTAINER
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code KPE·May 2, 2013
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.,·Product code CBK·August 27, 2014
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 20, 2011
PATIENT INFORMATION CENTER IX
FDA Adverse Event
Death
·PHILIPS MEDICAL SYSTEMS·Product code MHX·March 15, 2023
VERCISE CARTESIA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·June 21, 2023