88 results · 21ms · Sources: EU EUDAMED, US FDA

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SLIT LAMP, Model: YF-100

FDA 510(k)
FDA Class 2 ·Ophthalmic

THREADED STEINMANN PINS, DOUBLE END TROCAR POINT

FDA UDI
Biomet Orthopedics, LLC·00887868016561·

CHARTIS CONSOLE

FDA 510(k)
FDA Class 2 ·Anesthesiology

MEDIBYTE, MODEL MP8

FDA 510(k)
FDA Class 2 ·Anesthesiology

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code OTN·June 11, 2013

SENSOR, MMT-7002C, 10PK, GLUCOSE, BSA, 17L

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code MDS·July 8, 2011

REVEAL LINQ

FDA Adverse Event
Malfunction ·IPG MFG SWITZERLAND·Product code DSI·October 10, 2014

AMPLATZ EXTRA-STIFF SUPPORT WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·April 15, 2021

UNKNOWN

FDA Adverse Event
Injury ·COOK INC·Product code DQX·July 2, 2024

BENTSON STRAIGHT FIXED CORE WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·August 12, 2024

INSYTE AUTOGUARD BL 22GA X 1.0IN

FDA Adverse Event
Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·November 23, 2020

AMPLATZ EXTRA-STIFF SUPPORT WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·April 25, 2022

SAFE-T-J AMPLATZ EXTRA-STIFF SUPPORT WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·May 3, 2024

BENTSON STRAIGHT FIXED CORE WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·June 4, 2024

SAFE-T-J AMPLATZ EXTRA-STIFF SUPPORT WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·September 1, 2022

BENTSON STRAIGHT FIXED CORE WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·October 8, 2024

LUNDERQUIST-RING TORQUE WIRE GUIDE

FDA Adverse Event
Injury ·COOK INC·Product code DQX·September 28, 2021

LUCAS 3 CHEST COMPRESSION SYSTEM

FDA Adverse Event
Death ·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024

SAFE-T-J ROSEN CATHETER EXCHANGE WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·October 7, 2022

LUCAS 3 CHEST COMPRESSION SYSTEM

FDA Adverse Event
Death ·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024