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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