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NICOLET SUBDERMAL NEEDLE

FDA Adverse Event
Malfunction ·NICOLET BIOMEDICAL, INC.·Product code GXE·June 28, 1996

GE 8 SLICE CT SCANNER

FDA Adverse Event
Malfunction ·G.E. HEALTHCARE·Product code JAK·June 12, 2013

MEDISELECT II

FDA Adverse Event
Malfunction ·GCE, S.R.O.,·Product code CAN·May 2, 2024

MEDISELECT II

FDA Adverse Event
Malfunction ·GCE, S.R.O.,·Product code CAN·May 2, 2024

MEDITEC

FDA Adverse Event
Malfunction ·GCE, S.R.O.·Product code CAN·May 2, 2024

MEDISELECT II

FDA Adverse Event
Malfunction ·GCE, S.R.O.,·Product code CAN·May 2, 2024

MEDIREG II

FDA Adverse Event
Malfunction ·GCE, S.R.O.,·Product code CAN·May 2, 2024

G.E. MEDICAL

FDA Adverse Event
Malfunction ·G.E. MEDICAL·Product code DRT·January 26, 2001

MEDIVITOP

FDA Adverse Event
Malfunction ·GCE, S.R.O.·Product code CAN·May 16, 2025

HTG CASING

FDA Adverse Event
Malfunction ·G.E. MEDICAL SYSTEMS·Product code ITY·March 25, 2004

G.E. - MAC LAB

FDA Adverse Event
Malfunction ·G.E. MED SYS·Product code DQK·January 24, 2002

GENERAL ELECTRIC TREADMILL

FDA Adverse Event
Malfunction ·G.E. MEDICAL SYSTEMS·Product code IOL·January 23, 2006

GE INNOVA 2000

FDA Adverse Event
Malfunction ·G.E. MEDICAL SYSTEMS·Product code IZO·September 10, 2002

PORTABLE X-RAY MACHINE AMX-110

FDA Adverse Event
Malfunction ·G.E. MEDICAL SYSTEMS·Product code IZL·February 9, 1993

SOLAR 8000M

FDA Adverse Event
Malfunction ·G.E. MARQUETTE MEDICAL SYSTEMS·Product code MHX·May 21, 2002

SOLAR 9500

FDA Adverse Event
Malfunction ·G.E. MARQUETTE MEDICAL SYSTEMS·Product code MHX·May 21, 2002

REAGENT RED BLOOD CELLS 0.8% RESOLVE PANEL A

FDA Adverse Event
Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code KSZ·November 8, 2016

VIVID S6

FDA Adverse Event
Malfunction ·G.E MEDICAL SYSTEMS ISRAEL LTD.·Product code IYN·September 24, 2020

VIVID I

FDA Adverse Event
Malfunction ·G.E MEDICAL SYSTEMS ISRAEL LTD.·Product code ITX·February 5, 2020

VIVID I BT10*020473V

FDA Adverse Event
Malfunction ·G.E MEDICAL SYSTEMS ISRAEL LTD.·Product code IYO·January 28, 2021