10 results · 19ms · Sources: EU EUDAMED, US FDA

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Hair Regrowth Cap (Model: T-119-HRC)

FDA 510(k)
FDA Class 2 ·Physical Medicine

Medical X-ray Green / MXG Film

FDA UDI
CARESTREAM HEALTH, INC.·40889975253349·Medl X-ray Green/MXG Film 13X18cm 100SH

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197182348·Guyon-Bougies, acutely curved, 35.5 c...

Longeviti ClearFit Cranial Implant

FDA 510(k)
FDA Class 2 ·Neurology

HOFFMANN II ROD TO WIRE COUPLING

FDA 510(k)
FDA Class 2 ·Orthopedic

DYNESYS HA PEDICLE+SET SCREW 6.4X50

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code NQP·December 1, 2008

CAREASSIST BED

FDA Adverse Event
Malfunction ·HILL-ROM INC·Product code FNL·August 3, 2011

TREK CORONARY DILATATION CATHETER

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code LOX·July 29, 2013

SMART FLEX 9x60 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.

FDA Enforcement
Class II ·Ongoing·Cordis Corporation·November 24, 2021

Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models are not available in the US: models E103, E111, F102, F103, F110, F111. Sterilized using ethylene oxide. Product Usage: This family of implantable cardioverter defibrillators (ICDs) provide a variety of therapies including: -Ventricular tachyarrhythmia therapy, which is used to treat rhythms associated with sudden cardiac death such as VT and VF; -Bradycardia pacing, including adaptive rate pacing, to detect and treat bradyarrhythmias and to provide cardiac rate support after defibrillation therapy. Boston Scientific implantable cardioverter defibrillators (ICDs) are indicated to provide ventricular antitachycardia pacing (ATP) and ventricular defibrillation for automated treatment of life-threatening ventricular arrhythmias

FDA Enforcement
Class II ·Terminated·Boston Scientific CRM Corp·October 29, 2014