8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
HENKE DISPOSABLE SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
STRADIS
FDA UDI
STRADIS MEDICAL, LLC·M75268215371·CUSTOM SURGICAL KIT ENDOVENOUS PACK
MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005
FDA 510(k)
FDA Class 2
·Neurology
Nightwear Aligners
FDA 510(k)
FDA Class 2
·Dental
TOTAL HIP BALL 28MM +0
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.-1818910·Product code JDI·May 20, 2014
UNKNOWN RIGHT STRYKER KNEE
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·October 24, 2012
HEART START XL
FDA Adverse Event
Malfunction
·AGILENT TECHNOLOGIES, INC.·Product code MKJ·August 26, 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