29 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IDRIVE ULTRA POWERED HANDLE ENDO GIA ADAPTER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EGIA 45 ARTICULATING MED/THICK SULU
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·December 9, 2015
Aequalis™ Adjustable Reversed
FDA UDI
TORNIER, INC.·00846832068227·
SMARTPIN
FDA UDI
Conmed Corporation·10845854015476·SMARTPIN SELF-REINFORCED TECHNOLOGY, Ø1.5 X 10 MM
SMARTPIN
FDA UDI
Conmed Corporation·10845854015473·SMART PIN, DIAMETER 1.5 X 10MM
JOBST UltraSheer
FDA UDI
BSN MEDICAL, INC.·00035664215101·ULTRA SHEER 20-30 MM HG KNEE HIGH CLOSED TOE LA...
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515234543·Adson-Brown Bipolar Forceps, 4 3/4"
BD SYRINGE 3ML LL 200 S/C
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·November 13, 2024
X SERIES
FDA UDI
Zoll Medical Corporation·00847946059552·X SERIES MONITOR/DEFIBRILLATOR, 3/5 LEAD, SPO2,...
X SERIES
FDA UDI
Zoll Medical Corporation·00847946018511·Defibrillator ,X SERIES MONITOR/DEFIBRILLATOR, ...
X SERIES
FDA UDI
Zoll Medical Corporation·00847946014803·Defibrillator ,X SERIES MONITOR/DEFIBRILLATOR, ...
Cervical Interbody 15mm x 13mm x 10mm Packaging
FDA UDI
XENCO MEDICAL LLC·B064XM11215101·Cervical Interbody 15mm x 13mm x 10mm
X SERIES
FDA UDI
Zoll Medical Corporation·00847946099404·Defibrillator ,X SERIES MONITOR/DEFIBRILLATOR, ...
BD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·April 3, 2024
CancelleX™ 15mm x 13mm x 10mm Cervical Interbody
FDA UDI
XENCO MEDICAL LLC·B064XM3D31215101·
UNI-T UNI-THREAD SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FRACTIONAL SKIN RESURFACING (FSR) APPLICATOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY·Product code FMF·October 18, 2024
ACCENT DR RF
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTN·May 21, 2013