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

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Masimo O3 Regional Oximeter System

FDA 510(k)
FDA Class 2 ·Cardiovascular

O3 PEDIATRIC SENSOR

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MUD·August 20, 2022

O3 PEDIATRIC SENSOR

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MUD·August 19, 2022

ROOT

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code MWI·September 20, 2018

LEONE SPA

FDA UDI
LEONE SPA·08033707017776·CALIBRA 1ST MOLAR BANDS n.LR 26

TIPI

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

AMERITUS ENTRAL (TM) ENTERAL FEEDING TUBE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·July 24, 2017

CART 9733856 S7 STAFF ASSEMBLED 110V

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·February 18, 2020

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·November 24, 2016

ELECTRIC TRANSTAR STRETCHER

FDA Adverse Event
Malfunction ·HILL-ROM INC.·Product code INK·July 6, 2011

MARYLAND BIPOLAR FORCEPS INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 10, 2013

AFFINITY 4

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code HDD·September 10, 2008

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·February 18, 2017

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·November 4, 2016

PRODIGY POCKET

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·November 4, 2016

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·February 18, 2017

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·September 12, 2016

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·August 12, 2016

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·March 5, 2018