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