10,000 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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PROLENE
FDA UDI
ETHICON, LLC·10705031049017·Polypropylene Non-absorbable Synthetic Surgical...
PMH 1000 HEATED HUMIDIFIER
FDA 510(k)
FDA Class 2
·Anesthesiology
PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPY
FDA 510(k)
FDA Class 2
·Anesthesiology
PROLENE MESH (PMH)
FDA Adverse Event
Injury
·ETHICON·Product code FTL·March 9, 2017
MESH SOFRADIM - PARIETEX COMPOSITE MESH
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION SAS·Product code FTL·August 24, 2020
HEPARIN 100 UNITS/ML
FDA Adverse Event
Injury
·Product code NZW·May 1, 2008
KINETRA
FDA Adverse Event
Death
·MEDTRONIC NEUROMODULATION·Product code MHY·March 18, 2020
FENIX CONTINENCE RESTRORATION SYSTEM
FDA Adverse Event
Injury
·TORAX MEDICAL, INC.·Product code PMH·May 17, 2016
KINETRA
FDA Adverse Event
Death
·MEDTRONIC NEUROMODULATION·Product code MHY·September 9, 2013
HEARTWARE
FDA Adverse Event
Injury
·HEARTWARE-MEDTRONIC·Product code DSQ·May 29, 2018
OMNIPOD 5 CONTROLLER
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code QFG·March 23, 2026
HEARTWARE MEDTRONIC
FDA Adverse Event
Injury
·Product code DSQ·April 27, 2021
ETHICON INC.
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·September 10, 2008
ARROW
FDA Adverse Event
Injury
·ARROW·Product code FOZ·February 3, 2017
REMODULIN PUMP
FDA Adverse Event
Injury
·UNKNOWN·Product code FRN·June 6, 2023
HICKMAN CATHETER
FDA Adverse Event
Injury
·BARD ACCESS SYSTEMS, INC.·Product code LJS·May 24, 2023
HEARTWARE
FDA Adverse Event
Injury
·HEARTWARE-MEDTRONIC·Product code DSQ·May 17, 2018
HEPARIN PREFILLED SYRINGE 1:100
FDA Adverse Event
Death
·COVIDIEN·Product code NZW·May 28, 2008
COOK 5FR MICROPUNCTURE
FDA Adverse Event
Malfunction
·Product code DYB·July 24, 2008
PERCLOSE
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code MGB·August 7, 2015