31 results · 21ms · Sources: EU EUDAMED, 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