BEUDAMED
    88 results · 28ms · Sources: EU EUDAMED, US FDA

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    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·HeartSync Multifunction Disposable Single-Use AED Defibrillator Pads

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·HeartSync Multifunction Disposable Single-Use AED Defibrillator Pads

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·HeartSync Multifunction Disposable Single-Use Defibrillator Pads

    Paradigm

    FDA UDI
    Proprio, Inc.·00850042604038·Paradigm Surgical Instrument Tray

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377046901·RELINE-O Trial, 11mm H Lamina N L-pop

    Zavation

    FDA UDI
    Zavation LLC·00842166131552·Ti3Z CIF 12mmx14mmx7mm -0 deg

    4.0mm Tap Cann AO 125mm

    FDA UDI
    Osteocentric Technologies, Inc.·00810074306225·4.0mm Tap Cann AO 125mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694010788·1.0mm Pilot Drill, J-latch

    MicroAire®

    FDA UDI
    Microaire Surgical Instruments LLC·00847399000866·SMALL SAGITTAL SAW BLADE, 4.3mm X 15mm X 0.5mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694005616·1.6mm Pilot Drill, Manual

    iNAP

    FDA UDI
    SOMNICS, INC.·04719878320115·iNAP Saliva Container

    JEWELERS PRECISION FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896059351·JEWELERS PRECISION FORCEPS #PP SERRATED HANDLE

    PROFEMUR GLADIATOR Thin HA Classic Hip Stem with Collar

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PHYSICA KR LINER

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code MBH·December 20, 2022

    Stent, Renal

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC AVE BRIDGE EXTRA SUPPORT OVER THE WIRE RENAL STENT SYSTEM

    Replacement Heart-Valve

    FDA Pre-Market Approval
    FDA Class 3 ·EDWARDS PRIMA PLUS STENTLESS BIOPROSTHESIS MODEL 2500P

    SMR HUMERAL HEAD DIA. 46MM

    FDA Adverse Event
    Other ·LIMACORPORATE S.P.A.·Product code KWT·March 5, 2014

    BINAXNOW¿ COVID-19 AG CARD

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·January 4, 2022

    BINAXNOW¿ COVID-19 AG CARD

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·January 4, 2022

    LMA SUPREME SIZE 3

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAE·July 9, 2024