22 results · 25ms · 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.

XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINT

FDA 510(k)
FDA Class 2 ·Radiology

Axiom® Mills Sump

FDA UDI
AXIOM MEDICAL, INCORPORATED·M6651111670·Dual Lumen, Mediastinal, Round, Silicone, Open Tip

XSE

FDA 510(k)
FDA Class 2 ·Dental

PRESEP OLIGON OXIMETRY CATHETERS (16 CM, W/HEPARIN), (20CM, W/HEPARIN)

FDA 510(k)
FDA Class 2 ·Cardiovascular

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 8, 2025

QUICK CHECK ONE

FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·May 9, 1997

QUICK CHECK ONE

FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·December 4, 1996

QUICK CHECK ONE

FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·March 11, 1997

PROGRASP FORCEPS INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·August 5, 2014

ACHIEVA 1.5T NEW

FDA Adverse Event
Injury ·PHILIPS HEALTHCARE·Product code LNH·May 8, 2013

SERIES 20000 LEGACY

FDA Adverse Event
Other ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 26, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·August 14, 2008

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 6, 2015

PEDIASAT

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES PR·Product code DRE·December 10, 2025

EDWARDS OXIMETRY CENTRAL VENOUS CATHETER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code DXG·January 7, 2025

EDWARDS OXIMETRY CENTRAL VENOUS CATHETER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES PR·Product code DQE·March 27, 2025

EDWARDS OXIMETRY CENTRAL VENOUS CATHETER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code DXG·January 7, 2025

QUICK CHECK ONE

FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·November 19, 1996

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 8, 2016

QUICK CHECK ONE

FDA Adverse Event
Injury ·DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·February 12, 1997