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

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TRC-PASTE

FDA 510(k)
FDA Class 2 ·Dental

Starbond CoS

FDA UDI
S & S Scheftner GmbH·04260207854301·Powder 16, 5kg

AF541

FDA UDI
Respironics, Inc.·00606959046672·AF541 SE UTN, Capstrap, EXTRA SMALL

ROCHE ELECSYS FOLATE RBC; ROCHE ELECSYS FOLATE RBC CALSET

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

TRIDENT ACETABULAR SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

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

MAXGUARD PRE-SLIT INJECTION PORT

FDA Adverse Event
Malfunction ·CAREFUSION CORPORATION·Product code FPA·May 1, 2013

FORTIFY ST DR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·October 1, 2014

PARIETEX COMP 20X15CM W THR X1

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION·Product code FTL·June 9, 2011

ULTRAFLEX DUO HIGH FLUID CART - REFURBISHED

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

PERIPHERAL NERVE BLOCK SUPPORT TRAY

FDA Adverse Event
Malfunction ·I-FLOW, LLC·Product code CAZ·October 1, 2014

EVAC STATION

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

CONTINUOUS TRAY WITH 100MM NEEDLE, STIMULATING

FDA Adverse Event
Malfunction ·I-FLOW LLC·Product code CAZ·October 2, 2014

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

CONTINUOUS TRAY WITH 100MM NEEDLE 4IN ECHO NEE

FDA Adverse Event
Malfunction ·I-FLOW LLC·Product code CAZ·October 3, 2014

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