9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEART NEBULIZER #100609
FDA 510(k)
FDA Class 2
·Anesthesiology
SPINNING SPIROS® CLOSED MALE LUER, PURPLE CAP
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·May 30, 2019
SPINNING SPIROS® CLOSED MALE LUER, PURPLE CAP
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·May 30, 2019
LUBRICATING JELLY
FDA 510(k)
FDA Class 1
·General Hospital
RAINCOAT
FDA 510(k)
FDA Class 1
·Anesthesiology
TECNIS 1-PIECE
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HQL·February 15, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·January 11, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·UNKNOWN·Product code CAW·July 29, 2014
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·December 6, 2024