8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTEVENT ATOMIZER/NEBULIZER AEROSOL
FDA 510(k)
FDA Class 1
·Anesthesiology
Legacy
FDA UDI
Gc Orthodontics America Inc.·E53582262500001·LEGACY 1. MOLAR UPR LFT SZ 25
Shield System
FDA 510(k)
FDA Class 2
·Radiology
GETINGE 800HC- SERIES STEAM STERILIZER
FDA 510(k)
FDA Class 2
·General Hospital
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2014
ULTRACISION CURVED BLADE 10CM
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GEI·November 27, 2007
APPLIC-INSTR F/STERNAL ZIPFIX
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code JDQ·November 7, 2012
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