12 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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XPS Nexus System, XPS Nexus Foot Control, XPS Nexus IV Pole
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Oticon
FDA UDI
Oticon A/S·05707131280350·NERA2 PRO TI, BTE 13 WL 85 CBE DEMO
NEEDLE 18X1 RB
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·August 12, 2024
NEEDLE 18X1 RB
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·September 20, 2024
ATHENA MULTI-LYTE BORRELIA VLSE-1/PEPC10 PLUS TEST SYSTEM
FDA 510(k)
FDA Class 2
·Microbiology
OPEN BREAST COIL (OBC) WITH BIOPSY PLATES
FDA 510(k)
FDA Class 2
·Radiology
AIRVO2 HUMIDIFIER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·March 6, 2016
PROMUS ELEMENT ?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 6, 2013
ACCURUS 800CS
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 17, 2011
LEAD MODEL UNKNOWN
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·September 3, 2008
SURETRAK¿ II UNIVERSAL TRACKER, LARGE PASSIVE FIGHTER
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code OLO·May 22, 2024
ADULT BI-LEVEL INSPIRATORY HEATED BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·February 3, 2016