31 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODIFICATION TO CONTOUR POLARIS URETERAL STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Latitude™ EV
FDA UDI
TORNIER, INC.·00846832002863·Humeral Stem - Coated
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481114113·LOCATOR R-Tx Abutment for 3.4mm External Hex Im...
Cardiovascular Procedure Kit
FDA UDI
Terumo Cardiovascular Systems Corporation·00699753507401·
MEDART 520 COOLING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
N LATEX CYSTATIN C
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523134625·5.0mm X 25mm Rescue Hex Screw
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523134632·5.0mm X 30mm Rescue Hex Screw
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523117871·5.0mm X 30mm Rescue Screw
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523134618·5.0mm X 20mm Rescue Hex Screw
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523134649·5.0mm X 35mm Rescue Hex Screw
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523117888·5.0mm X 35mm Rescue Screw
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523117857·5.0mm X 20mm Rescue Screw
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523117864·5.0mm X 25mm Rescue Screw
21GX.75IN. BD VACUTAINER® WINGED SAFETY PBBCS WITH 12 IN TUBING
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·November 27, 2017
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET PRE-ATTACHED HOLDER 23G NEEDLE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 3, 2017
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·January 31, 2024
APEX¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·April 2, 2013
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 9, 2011
AED PLUS
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP·Product code MKJ·April 16, 2008