10,000 results
·
59ms
·
Sources: EU EUDAMED, US FDA
CRW®
FDA UDI
INTEGRA LIFESCIENCES CORPORATION·10381780252146·Depth Stop, Plastic, 2.1mm
CC08 Ion chamber
FDA UDI
IBA Dosimetry GmbH·EIBADS210000·CC08 Ion chamber: 0.08 ccm, shonka plastic, w...
CC08 Ion chamber
FDA UDI
IBA Dosimetry GmbH·EIBADS211000·CC08 Ion chamber: 0.08 ccm, shonka plastic, w...
312/DS-039/2-1 DS-039/2 basic element & curtain (no pivotal arm)
Device
EU MDR
·
Eu Md Class 1
·Kenex (Electro-Medical) Limited·On the market
KENEX
FDA UDI
KENEX (ELECTRO-MEDICAL) LIMITED·05055449405911·312/DS-039/2-1
SPYSCOPE DS II ACCESS & DELIVERY CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FBN·November 14, 2022
THORATEC® HEARTMATE 3® LVAS IMPLANT KIT
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·January 9, 2025
EDWARDS NOVAFLEX+ DELIVERY SYSTEM
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·November 18, 2015
EDWARDS NOVAFLEX+ DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code NPT·November 17, 2015
EX-PRESS GLAUCOMA FILTRATION DEVICE
FDA Adverse Event
Malfunction
·OPTONOL LTD.·Product code KYF·May 21, 2019
EX-PRESS GLAUCOMA FILTRATION DEVICE
FDA Adverse Event
Malfunction
·OPTONOL LTD.·Product code KYF·July 9, 2019
BAERVELDT SHUNT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYF·March 15, 2016
INOMAX DS (DELIVERY SYSTEM)
FDA Adverse Event
Injury
·INO THERAPEUTICS, LLC/IKARIA·Product code MRN·November 2, 2011
EX-PRESS GLAUCOMA FILTRATION DEVICE
FDA Adverse Event
Malfunction
·OPTONOL LTD.·Product code KYF·July 15, 2019
EDWARDS NOVAFLEX+ DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code NPT·September 4, 2014
DLT TS CER HD 12/14 32MM +5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·August 23, 2021
MICRA¿ AV2
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code PNJ·August 8, 2024
MICRA
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code PNJ·January 17, 2025
EX-PRESS GLAUCOMA FILTRATION DEVICE
FDA Adverse Event
Malfunction
·OPTONOL LTD.·Product code KYF·January 17, 2019
BD PYXIS¿ MEDSTATION¿ ES
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·October 8, 2025