BEUDAMED
    34 results · 23ms · Sources: EU EUDAMED, US FDA

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    Disposable Pre-calibrated Suction

    FDA 510(k)
    FDA Class 2 ·Neurology

    Shannon Recta Larga Round Shank

    FDA UDI
    Gebr. Brasseler GmbH & Co. KG·14053613289600·

    HHM

    FDA UDI
    Oticon A/S·05707131351548·G500 SC, BTE PP 13 2.4G 105 C047 TAR HHM

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704066941·CODMAN SLIM-LINE Aneurysm Clip Reinforcing Angl...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776194734·RENAL VEIN RETRACTOR DEEP WITH LOOP HANDLE CU...

    Symmetry Cushing

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482057735·Symmetry® Retractor, Cushing Vein, 14 in

    MEDIS 55MP1H SINGLE-HEAD MEDICAL DIAGNOSTIC DISPLAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    FP(HEXAFOCON A)RGP CONTACT LENS SPHERICAL/ASP(HEXAFOCON A)RGP CONTACT LENS ASPHERICAL

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LONG NAIL KIT R2.0, STST, RIGHT 11X360MM X 125

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·May 25, 2010

    GE OEC 9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 21, 2008

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 26, 2013

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 5, 2011

    AORTIC EXCLUDER AAA ENDOPROSTHESIS (C3)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·June 25, 2020

    UNKNOWN SHOULDER GLENOSPHERE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWS·March 23, 2018

    UNKNOWN SHOULDER HUMERAL CUP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWS·March 23, 2018

    UNKNOWN SHOULDER METAGLENE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code HSD·March 21, 2018

    UNKNOWN SHOULDER LOCKING SCREW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWS·March 21, 2018

    UNKNOWN SHOULDER LOCKING SCREW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code HWC·March 21, 2018

    UNKNOWN SHOULDER HUMERAL STEMS

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWS·October 25, 2018

    UNKNOWN SHOULDER HUMERAL BODY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWS·October 25, 2018