439 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0104020·Caddie, Large, 30mm
TiWAVE L Lumbar Cage System
FDA UDI
Kalitec Direct LLC·B07323K0104020·Caddie, Large, 30mm
SMOOTH-FLO CIRCUIT
FDA 510(k)
FDA Class 2
·Anesthesiology
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964150302·Endo Carry-on Procedure Kit Includes Intercept ...
ROLLO 104X40X16E*31*ASCARD-3U
FDA UDI
AB MEDICA GROUP, S.A.·08428763004417·
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0100020·Tap, 4.5mm Cann, Quarter Square
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0100420·Assembly, Caddie, Adjustable Cross Links
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0100020·Caddie, 1-3 Level Plates
SCREENERS PHENCYCLIDINE (PCP) TEST, DRUGSCREEN DIP PHENCYCLIDINE (PCP) TEST
FDA 510(k)
FDA Unclassified
·Unknown
CONTOUR POLARIS URETERAL STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ORBERA365 INTRAGASTRIC BALLOON SYSTEM
FDA Adverse Event
Malfunction
·APOLLO ENDOSURGERY·Product code LTI·February 13, 2024
PERCUFLEX PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FAD·March 13, 2025
PERCUFLEX? PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FAD·March 13, 2025
PERCUFLEX? PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FAD·March 13, 2025
ADVANIX BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 24, 2023
AGILE? ESOPHAGEAL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code ESW·August 20, 2025
FREESTYLE
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC., USA·Product code LFR·May 11, 2007
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·March 19, 2013
SEXTANT
FDA Adverse Event
Malfunction
·Product code KWP·March 1, 2011
ADVANIX BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 24, 2023