12 results
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33ms
·
Sources: EU EUDAMED, US FDA
TMX-70 TREADMILL
FDA 510(k)
FDA Class 1
·Physical Medicine
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209105106·
Guardian 1000
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BLEAS ESIRIUC ANAESTHSIA SYSTEM, MODELS 3000, 2000
FDA 510(k)
FDA Class 2
·Anesthesiology
RA CATH SET: 20 GA X 1-1/2"
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC·Product code DQX·April 18, 2014
NAVISTAR¿ ELECTROPHYSIOLOGY CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·November 29, 2012
PUMP MMT-715NAS PRDGM INS V2.1 SK EN
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·September 28, 2010
2.4MM TI VA LOCKING SCREW STARDRIVE 18MM-STERILE
FDA Adverse Event
Injury
·SYNTHES SELZACH·Product code HRS·March 23, 2017
2.4MM TI VA LOCKING SCREW STARDRIVE 22MM-STERILE
FDA Adverse Event
Injury
·SYNTHES SELZACH·Product code HRS·March 23, 2017
2.4MM TI VA LOCKING SCREW STARDRIVE 18MM-STERILE
FDA Adverse Event
Injury
·SYNTHES SELZACH·Product code HRS·March 23, 2017
2.4MM TI VA LOCKING SCREW STARDRIVE 18MM-STERILE
FDA Adverse Event
Injury
·SYNTHES SELZACH·Product code HRS·March 23, 2017
2.4MM TI VA LOCKING SCREW STARDRIVE 20MM-STERILE
FDA Adverse Event
Injury
·SYNTHES SELZACH·Product code HRS·March 23, 2017