52 results · 25ms · Sources: EU EUDAMED, US FDA

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ULTRA HDL

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

S45 (OCUFILCON A) SPHERICAL, ASPHERICAL, TORIC AND MULTIFOCAL SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, FULLY-

FDA 510(k)
FDA Class 2 ·Ophthalmic

ADVANTAGE MARIJUANA (THC) AND COCAINE HOME DRUG TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

ZIMMON BILIARY STENT SET

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·October 25, 2018

ZIMMON BILIARY STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·August 14, 2018

ZIMMON BILIARY STENT SET

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·January 9, 2019

BD PHOENIX¿ SMIC-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

ZILVER 635 BILIARY SELF EXPANDING METAL STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·October 22, 2021

ZIMMON BILIARY STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·December 11, 2018

OASIS ONE ACTION STENT INTRODUCTION SYSTEM

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·December 11, 2018

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·August 16, 2018

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 11, 2013

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·April 12, 2011

COMPLETE LEAD SET AAMI

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DRX·May 22, 2008

BD PHOENIX¿ SMIC/ID-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024