52 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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