15 results · 20ms · Sources: EU EUDAMED, US FDA

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Atellica IM Ferritin Assay

FDA 510(k)
FDA Class 2 ·Immunology

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704293753·

MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

ONCO TRAC MODEL 1, 2, 4

FDA 510(k)
FDA Class 2 ·Radiology

3 ML BD SYRINGE WITH BD LUER-LOK¿ TIP

FDA Adverse Event
Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·March 12, 2018

BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM

FDA Adverse Event
Malfunction ·BD SUZHOU (MDS)·Product code FOZ·January 21, 2025

ACCU-CHEK ® MOBILE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 14, 2014

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·July 21, 2011

CORTSCR Ø1.5 SELF-TAP L6

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code MQN·June 15, 2013

3 ML BD LUER-LOK¿ DISPOSABLE SYRINGE WITH BD LUER-LOK¿ TIP

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 20, 2018

OPEN-END FLEXI-TIP URETERAL CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KOD·February 6, 2020

OPEN-END URETERAL CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KOD·February 7, 2020

BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM

FDA Adverse Event
Malfunction ·BD SUZHOU (MDS)·Product code FOZ·January 14, 2025

OPEN-END URETERAL CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KOD·December 5, 2019

Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)

FDA Enforcement
Class II ·Ongoing·Medtronic Inc.·November 29, 2017