16 results · 22ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

EOGas 4 Ethylene Oxide Gas Sterilizer

FDA 510(k)
FDA Class 2 ·General Hospital

HNM Women Care

FDA UDI
HNM STAINLESS, LLC.·00812171027935·PESSARY, CUP #7, W/O SUPPORT, 85/52mm

BD DISCARDIT¿ SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·November 14, 2022

BD DISCARDIT¿ SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·November 14, 2022

BD DISCARDIT¿ SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·November 14, 2022

BD DISCARDIT¿ SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·November 14, 2022

BD DISCARDIT¿ SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·November 14, 2022

SYNTHES (USA) 3.5/4.5MM LCP MEDIAL PROXIMAL TIBIA PLATES

FDA 510(k)
FDA Class 2 ·Orthopedic

AFFINITY PIXIE ARTERIAL FILTER WITH BALANCE BIOSURFACE

FDA 510(k)
FDA Class 2 ·Cardiovascular

BD DISCARDIT¿ SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·August 16, 2022

BD DISCARDIT¿ SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·November 14, 2022

GYNECARE TVT OBURATOR SYSTEM

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·June 6, 2013

ENDOPATH** ENDOSCOPIC

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 6, 2011

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008

MEDTRONIC DUAL CHAMBER TEMPORARY EXTERNAL PACEMAKER 510(K) K150246

FDA Adverse Event
Death ·MEDTRONIC, INC.·Product code DTE·February 10, 2021

TREVO XP PROVUE 4MM X 30MM

FDA Adverse Event
Injury ·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code NRY·July 24, 2020