12 results · 20ms · Sources: EU EUDAMED, US FDA

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SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 29, 2024

11MM/130 DEG TI CANN TROCH FIXATION NAIL 320MM/LEFT-STER

FDA Adverse Event
Malfunction ·SYNTHES MONUMENT·Product code HSB·April 29, 2013

ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORP.·Product code LZG·April 13, 2011

MTOME ST HOLSTER/CABLES

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC·Product code KNW·July 25, 2008

CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

FDA Adverse Event
Injury ·COOK INC·Product code FOZ·August 22, 2022

CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

FDA Adverse Event
Injury ·COOK INC·Product code FOZ·August 22, 2022

TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DQY·July 3, 2018

TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DQY·July 3, 2018

TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DQY·June 25, 2018

Catheter, intravascular, therapeutic, short-term less than 30 days

FDA Adverse Event
Malfunction ·COOK INC·Product code FOZ·November 10, 2022

1820334-2022-00399

FDA Adverse Event
Injury ·COOK INC·Product code LJS·March 16, 2022

CONNECTOR, 1/4" X 1/4" STRAIGHT WITH LUER LOCK PORT

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code OEZ·April 26, 2016