30 results · 29ms · Sources: EU EUDAMED, US FDA

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OCELOT CATHETER, OCELOT PIXL CATHETER, LIGHTBOX CONSOLE

FDA 510(k)
FDA Class 2 ·Cardiovascular

Gyrus ACMI

FDA UDI
Gyrus ACMI, LLC·00821925015470·HOUSE-TYPE SS WIRE LP

Reef TH

FDA UDI
Seaspine Orthopedics Corporation·10889981201890·Interbody, 11mm x 40mm x 18mm, 15 deg

Reef TA

FDA UDI
Seaspine Orthopedics Corporation·10889981193904·Interbody, 11mm x 40mm x 18mm, 15 deg

SLEEP APP

FDA 510(k)
FDA Class 2 ·Dental

DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM

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

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·February 19, 2016

IN00087 CLERMONT FERRAND PH

FDA Adverse Event
Death ·SORIN GROUP ITALIA·Product code DWF·March 7, 2014

SEDLINE KIT

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code MWI·January 8, 2017

ENDOTAK RELIANCE

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code NVY·October 3, 2014

STERIS SYSTEM 1E

FDA Adverse Event
STERIS CORPORATION - HOPKINS·Product code MED·May 31, 2013

COLLEAGUE PRE-P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 25, 2011

RADICAL-7

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·July 9, 2015