BEUDAMED
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    RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Affiniti

    FDA UDI
    TORNIER, INC.·00846832024551·HUMERAL HEAD TRIAL

    intellijoint HIP®

    FDA UDI
    Intellijoint Surgical Inc·00628184002414·Workstation, G2, Configured

    SR Facebow

    FDA UDI
    ORMCO CORPORATION·00889989023329·Facebow MINI-VEC SZ 1 .044 DIA

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659349742·3.5mm Proximal Tibia Plate 4 Holes Right ...

    e-vive NMES System; 2XL/3XL, Right, Bilateral Kit

    FDA UDI
    Motive Health, Inc.·00854691008506·e-vive NMES System; 2XL/3XL, Right, Bilateral Kit

    CURE IVIEW

    FDA UDI
    MEDITECH SPINE, LLC·B167900002410·

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167700002410·

    3.5mm Proximal Tibia Plate 4 Holes Right

    FDA UDI
    mahe medical gmbh·EMAH20002410040·3.5mm Proximal Tibia Plate 4 Holes Right

    3.5mm Proximal Tibia Plate 4 Holes Left

    FDA UDI
    mahe medical gmbh·EMAH20002410050·3.5mm Proximal Tibia Plate 4 Holes Left

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659349759·3.5mm Proximal Tibia Plate 4 Holes Left ...

    MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HARDYDISK, STREPTOMYCIN 10MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1700002410·

    CURE IVIEW

    FDA UDI
    MEDITECH SPINE, LLC·B167S1900002410·

    BONE SCREW Ø6,5 H.45MM

    FDA Adverse Event
    Malfunction ·LIMACORPORATE S.P.A.·Product code LPH·November 3, 2021

    Workstation, G2, Configured (P/N 000-0241)

    FDA Recall
    Terminated ·Intellijoint Surgical, Inc.·Product code OLO·June 28, 2019

    CUP: MPACT ACETABULAR SHELL 58 MULTI-HOLE

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·July 21, 2021

    MBT CEM KEEL TIB TRAY SZ4

    FDA Adverse Event
    Injury ·DEPUY IRELAND·Product code NJL·March 12, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·February 18, 2011