BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    CrossCLIP Implant System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814244·GENUMEDI PT SILVER L VII

    LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMY

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    POCKET SIZE RESUSCITATOR/MODEL: M16201R AND M16201A

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MATRIXMIDFACE SCREWDRIVER BLD HEX COUPLING/SELF-RETAIN/76MM

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·August 29, 2018

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 24, 2013

    ALTRX +4 NEUT 36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 23, 2011

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·August 26, 2008

    LARGE, RIGHT 16 POST AUG UHMWPE GLENOID

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·April 28, 2025