9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
FOX POST NASAL BALLOON CATHETER
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
Precept
FDA UDI
Nuvasive, Inc.·00887517370150·PRECEPT Rod, 40mm
ReLine
FDA UDI
Nuvasive, Inc.·00195377020758·RELINE-C Ti Rod, 3.5x40mm Straight
VARELISA MPO ANCA, MODEL 17648/17696
FDA 510(k)
FDA Class 2
·Immunology
Amethyst HP PTA OTW 0.035 Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
ACRYSOF
FDA Adverse Event
Injury
·ALCON LABORATORIES IRELAND LTD.·Product code HQL·May 14, 2014
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 20, 2012
PATIENT ROOM WALL SAVER RECL
FDA Adverse Event
Malfunction
·STRYKER CORP MEDICAL DIV·Product code FRK·September 10, 2010
Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018