60 results
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26ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HEARTSTART XL+DEFIBRILLATOR/MONITOR WITH END-TIDAL CARBON DIOXIDE MONITORING
FDA 510(k)
FDA Class 3
·Cardiovascular
INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK, INC.·Product code MAX·May 9, 2019
VARIAN, INC. ONTRAK TESTCUP AND ONTRAK TESTSTIK
FDA 510(k)
FDA Class 2
·Clinical Toxicology
CS 9300, CS 9300C
FDA 510(k)
FDA Class 2
·Radiology
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973936·UniTip High Resolution Catheter 14F
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973295·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970287·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970959·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970270·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970300·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970690·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970935·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973455·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970294·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970195·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970225·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970676·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970201·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970645·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970942·