BEUDAMED
    796 results · 21ms · Sources: EU EUDAMED, US FDA

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    Impulse AM Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ti-Fix OLIF Spacer

    FDA UDI
    Tyber Medical, LLC·M695P32100900·Ti-Fix OLIF Spacer 32 x 10 x 9 (mm) x 0 °

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869604154·MOSS Ti Rod, Ø5.5x90mm curved

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C30422100900·PEEK PLIF Spacer, 22 x 10 x 9mm, 0 deg

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C31422100900·Titanium PLIF Spacer, 22 x 10 x 9mm, 0 deg

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869621205·MOSS VRS Ti rod, Ø5.5x90mm, curved

    XLTEK EVOKED POTENTIAL HEADBOX, MODEL EP-4-RP (PROPOSED)

    FDA 510(k)
    FDA Class 2 ·Neurology

    AFX INTRODUCER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    XtraFix®

    FDA UDI
    Zimmer, Inc.·00889024081390·

    Widex

    FDA UDI
    Widex A/S·05706069691887·Widex BEYOND B-F2 (Metallic Blue ) 110, Telecoi...

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 29, 2014

    DISCOFIX STOPCOCKS

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL, INC.·Product code FMG·June 27, 2013

    AFT DIVERTED TUBE (3/4 FILLED)

    FDA Adverse Event
    Other ·MTF·Product code MBP·August 3, 2011

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 21, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 25, 2021