77 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANGIOSCULPT PTA SCORING BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)
FDA Adverse Event
Malfunction
·ANGIOSCORE, INC·Product code LIT·November 18, 2015
Mortez
FDA UDI
MEDTRONIC XOMED, INC.·00681490033527·PROSTHESIS 1112182 MORETZ CAM H/A FLPL
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089458837·
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
Malfunction
·INVAMEX·Product code ILS·May 15, 2013
DAILY ACTIVITY ASSIST DEVICE
FDA Adverse Event
Malfunction
·FOSHAN R. POON MEDICAL PRODUCTS CO., LTD.·Product code ILS·June 14, 2013
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
Malfunction
·INVAMEX·Product code ILS·June 20, 2013
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161121820400·Trial Head Ø28mm -3.5mm Green
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161121820410·Trial Head Ø28mm 0.0mm Yellow
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161121820420·Trial Head Ø28mm +4.0mm Orange
MAQUET FLOW-I C20, MAQUET FLOW-I C30, MODEL 66 77 200, 66 77 30
FDA 510(k)
FDA Class 2
·Anesthesiology
CANNABINOIDS URINE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ALL-IN-ONE-ALUMINUM COMMODE 4 PER CARTON 9153637754
FDA Adverse Event
Malfunction
·INVAMEX·Product code ILS·April 7, 2015
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
Malfunction
·INVAMEX·Product code INB·August 23, 2012
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
Malfunction
·INVAMEX·Product code ILS·March 20, 2013
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
Malfunction
·INVAMEX·Product code ILS·April 12, 2013
Femoral Sound
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215039653·
Trial Head
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215038397·
S-Type QR Fitting: Helios
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215039585·
IM Drill – Zimmer Hall Connection
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215039578·