55 results · 23ms · Sources: EU EUDAMED, US FDA

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TEMPLATE AND COUNTER-FIT

FDA 510(k)
FDA Class 2 ·Dental

Stainless Steel Wire

FDA UDI
Dentsply International Inc.·D001N0810170·Round 10ft

n/a

FDA UDI
Ortho Development Corporation·00822409075447·12/14 Press-Fit Broach 10x17

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014608976·GETINGE / SHAMPAINE 3" DELUXE

InTess L

FDA UDI
Kalitec Direct LLC·B07312K0310170·T-Handle, Fixed, 1/4" Square

PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT

FDA 510(k)
FDA Class 2 ·Neurology

RETRAX RETRACTING NEEDLE SYRINGE, SIZE 3CC

FDA 510(k)
FDA Class 2 ·General Hospital

DUO FLUID CART

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·December 21, 2017

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·August 31, 2018

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·April 24, 2013

PASSPORT 2 MONITOR

FDA Adverse Event
Malfunction ·MINDRAY DS USA, INC.·Product code MHX·August 22, 2014

2800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 14, 2011

ULTRAFLEX DUO HIGH FLUID CART - REFURBISHED

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·June 25, 2020

EVAC STATION

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·September 5, 2017

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·March 17, 2016

ULTRAFLEX DUO HIGH FLUID CART WITH SMOKE EVACUATOR

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·January 11, 2018

EVAC STATION

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·January 16, 2018

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·June 7, 2018

ULTRAFLEX DUO HIGH FLUID CART WITH SMOKE EVACUATOR

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·August 3, 2017

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·March 19, 2018