1,817 results
·
23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MAMMOREP LOOP MLE
FDA UDI
STERYLAB SRL·08033959221846·Repleaceable device for breast lesions localiza...
MAMMOREP LOOP MLE
FDA UDI
STERYLAB SRL·08033959221839·Repleaceable device for breast lesions localiza...
MAMMOREP LOOP MLE
FDA UDI
STERYLAB SRL·08033959221822·Repleaceable device for breast lesions localiza...
MAMMOREP LOOP MLE
FDA UDI
STERYLAB SRL·08033959221853·Repleaceable device for breast lesions localiza...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925036413·ACMI USA Elite System and USA Series Right Angl...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925038455·ACMI USA Elite System and USA Series Right Angl...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925038462·ACMI USA Elite System and USA Series Right Angl...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925038448·ACMI USA Elite System and USA Series Right Angl...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925038479·ACMI USA Elite System and USA Series Right Angl...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925038486·ACMI USA Elite System and USA Series Right Angl...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925036437·ACMI USA Elite System and USA Series Right Angl...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925038493·ACMI USA Elite System and USA Series Right Angl...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925036420·ACMI USA Elite system and USA Series Right Angl...
MW5072515
FDA Adverse Event
Malfunction
·September 27, 2017
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·October 1, 2022
MLE-26-012
FDA Adverse Event
Malfunction
·CIRCON CORP·Product code FAS·March 11, 2002
CUTTING LOOP
FDA Adverse Event
Malfunction
·ACMI NORWALK·Product code KNS·October 25, 2002
ACMI (MLE-24-012)
FDA Adverse Event
Other
·ACMI·Product code KNS·May 13, 2005
ACMI (MLE - 26 - 012)
FDA Adverse Event
Other
·ACMI·Product code FJL·July 11, 2005
MARA PROBE
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code MNB·May 12, 2022