1,072 results · 33ms · Sources: EU EUDAMED, US FDA

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SURGICAL KIT

FDA UDI
Sin Sistema de Implante Nacional S/A·07899995209290·KIT ROTARY EXPANDER

Custom Healthcare Systems Inc.

FDA UDI
Manus Medical, LLC·00811870031922·

KERASAVE

FDA UDI
AL.CHI.MI.A. SRL·08021118001408·Kerasave is a low salt, vitamin, amino acid, an...

IOLMASTER 700

FDA Adverse Event
Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·April 12, 2021

AUTOSTAINER LINK 48

FDA Adverse Event
Malfunction ·DAKO·Product code KPA·December 11, 2013

Fusion Anterior Instrument Set

FDA UDI
Xtant Medical Holdings, Inc.·00846468096298·Kerrison Rongeur

Fusion Anterior Instrument Set

FDA UDI
Xtant Medical Holdings, Inc.·00846468096281·Kerrison Rongeur

IOLMASTER XP

FDA Adverse Event
Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·July 12, 2021

TALENT AAA STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·May 13, 2016

ENDURANT STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·May 13, 2016

IOLMASTER

FDA Adverse Event
Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·March 3, 2016

COBALT¿ DR MRI SURESCAN¿

FDA Adverse Event
Malfunction ·MEDTRONIC EUROPE SARL·Product code LWS·March 31, 2026

CURITY GAUZE SPONGES, 16P1Y4" X 4", STERI

FDA Adverse Event
Malfunction ·MEDTRONIC / COVIDIEN·Product code GDY·December 20, 2016

BIO 701 CONTAINER WITH INSULATION

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code KER·December 7, 2017

IP BIOPSY CASSETTE II

FDA Adverse Event
Malfunction ·LEICA B IOSYSTEMS RICHMOND·Product code KER·November 17, 2011

IP BIOPSY CASSETTE II

FDA Adverse Event
LEICA BIOSYSTEMS·Product code KER·October 12, 2011

TISSUE-TEK UNI-CASSETTE

FDA Adverse Event
Malfunction ·SAKURA FINETEX USA·Product code KER·October 18, 2011

ABSORBATACK

FDA Adverse Event
Malfunction ·COVIDIEN SURGICAL·Product code GDW·April 21, 2026

RESTYLANE LYFT WITH LIDOCAINE

FDA Adverse Event
Injury ·GALDERMA Q-MED AB·Product code LMH·September 8, 2020

RESTYLANE SILK

FDA Adverse Event
Injury ·GALDERMA Q-MED AB·Product code LMH·September 8, 2020