11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Deklene MAXX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HHM
FDA UDI
Oticon A/S·05707131343314·G100, MINIRITE T 312 2.4G C093 HHM
BD SYRINGE 10ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·December 26, 2024
BD SYRINGE 10ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·December 26, 2024
ULTRASONIC SCALER
FDA 510(k)
FDA Class 2
·Dental
SPIRODOC
FDA 510(k)
FDA Class 2
·Anesthesiology
FIRST PICC PERIPHERALLY INSERTED CENTRAL CATHETER
FDA Adverse Event
Other
·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code LJS·October 8, 2008
PLUM A+ TRIPLE NEW 8
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·July 21, 2011
UNKNOWN M2A MAGNUM HIP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 27, 2013
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code ELC·April 29, 2020
NSK
FDA Adverse Event
Malfunction
·NAKANISHI INC.·Product code ELC·May 31, 2023