BEUDAMED
    13 results · 27ms · Sources: EU EUDAMED, US FDA

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    SAPHLIFT

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377097286·RELINE C Center Guide, Adj Crosslink

    EARGO

    FDA UDI
    Eargo, Inc.·00850010429090·EARGO Replacement Flexi Dome, Size Large

    247

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935105565·

    WV1417A DIGITAL X-RAY DIRECT IMAGING FLAT PANEL DETECTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    STATCLAVE G4 Chamber Autoclave

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEO·June 19, 2006

    GOBED II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 5, 2013

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 7, 2014

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·January 28, 2011