10 results · 23ms · Sources: EU EUDAMED, US FDA

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Revolution XR/d Wall Stand, Model Number 2291655, for Revolution XR/d Digital Radiographic Imaging Systems

FDA Recall
Terminated ·General Electric Med Systems·Product code 90LMA·November 21, 2002

Arndt

FDA UDI
COOK INCORPORATED·00827002119208·Arndt Airway Exchange Catheter

Arndt

FDA UDI
COOK INCORPORATED·00827002576254·Arndt Airway Exchange Catheter Set with Rapi-Fi...

NSK

FDA Adverse Event
Malfunction ·NAKANISHI INC·Product code EGS·December 18, 2017

IMPELLA CP EU

FDA Adverse Event
Injury ·ABIOMED, INC.·Product code OZD·December 14, 2023

ECT DEVICE THYMATRON SYSTEM IV (SOMATICS)

FDA Adverse Event
Injury ·SOMATICS, LLC.·Product code QGH·August 8, 2022

SOMATICS THYMATRON SYSTEM IV

FDA Adverse Event
Injury ·SOMATICS, LLC·Product code GXC·September 8, 2022

K-wire, Smooth Double-pointed 0.8 x 90mm, a component of the METASURG Capture Screw System The K-wire is used in conjunction with the 2.0 mm cannulated screws for the METASURG Capture Screw System. The K-wire is used by the physician to insert into the bone and to act as a guide for drilling, countersinking and installing screws

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·July 6, 2016

AEROAUTOCAT 2 WAVE

FDA Adverse Event
Malfunction ·ARROW INTL., INC.·Product code DSP·March 5, 2014

K-wire, Smooth Double-pointed 0.8 x 90mm, a component of the METASURG Capture Screw System The K-wire is used in conjunction with the 2.0 mm cannulated screws for the METASURG Capture Screw System. The K-wire is used by the physician to insert into the bone and to act as a guide for drilling, countersinking and installing screws

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code HXI·May 20, 2016