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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code HTO·October 21, 2008

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 12, 2011

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 3, 2013

UNKNOWN ENDO GIA INSTRUMENT

FDA Adverse Event
Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·September 14, 2023

QDOT MICRO

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·May 27, 2026

QDOT MICRO

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·April 28, 2026

QDOT MICRO

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·May 19, 2026

NGEN RF GENERATOR

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·December 16, 2025

AUTO SUTURE

FDA Adverse Event
Malfunction ·US SURGICAL PUERTO RICO·Product code GCJ·July 21, 2023

ENDO GIA

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·August 16, 2023

ENDO GIA ULTRA

FDA Adverse Event
Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·January 12, 2023

UNKNOWN SIGNIA EGIA ADAPTER

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·January 30, 2023

NGEN RF GENERATOR, JAPAN

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code LPB·April 21, 2023

QDOT MICRO

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·March 6, 2026

QDOT MICRO

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·February 6, 2026