406 results · 25ms · Sources: EU EUDAMED, US FDA

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TALON SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

N/A

FDA UDI
GEORGE TIEMANN & CO.·B58211029950·HOOK, SURGICAL, GENERAL & PLASTIC SURGERY

SHIKANI SPEAKING VALVE

FDA 510(k)
FDA Class 2 ·Anesthesiology

COLLATEK SHEET

FDA 510(k)
FDA Unclassified ·Unknown

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·March 29, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·May 27, 2021

SOFTCLIX ® LANCET DEVICE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 9, 2013

PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·September 19, 2014

EXTENSION SET

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·May 25, 2011

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 6, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·March 24, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·June 15, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·May 18, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·June 7, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·April 2, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·April 8, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·April 16, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·April 28, 2021

V60 VENTILATOR

FDA Adverse Event
Malfunction ·Product code MNT·November 24, 2020

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·July 2, 2021