10 results · 18ms · 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.

SAS SALMONELLA 0 GROUP E FACTORS 1,3,10,15,19,34 ANTISERUM

FDA 510(k)
FDA Class 2 ·Microbiology

HA Bone Screws

FDA UDI
ORTHOFIX SRL·18032568861891·OSTEOTITE SELF-DRILL.160/70 MM BONE SCREW THREA...

CT TrueView

FDA 510(k)
FDA Class 2 ·Radiology

POWDER FREE NITRILE EXAMINATION GLOVES, BLUE

FDA 510(k)
FDA Class 1 ·General Hospital

INSERT, BIPOLAR FORCEPS

FDA Adverse Event
Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code GEI·April 2, 2015

1723170-2019-02646

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·May 24, 2019

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 24, 2014

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 13, 2013

MEDISENSE OPTIUM

FDA Adverse Event
Malfunction ·Product code NBW·January 13, 2011

Marathon Flow Directed Micro Catheter, UltraFlow HPC Flow Directed Micro Catheter Marathon Flow: The device is intended to access periphera and neurovasculature for the controlled selective infusion of physician-specified therapeutics agents such as embolization materials and of diagnostic materials such as contrast media. UltraFlow HPC Flow: The device is intended for the controlled selective infusion of physician-specified pharmacologic agents or contrast media into the distal vasculature of the peripheral and neuroanatomy. It is not intended for use in the coronary vasculature. Catalog No. 105-5055V02 105-5055V02 105-5055V05 105-5065V02 105-5065V05 105-5066V02 105-5066V05

FDA Enforcement
Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·November 16, 2016