BEUDAMED
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    ULTRAPAK NEHA

    FDA 510(k)
    FDA Unclassified ·Unknown

    Atos Medical

    FDA UDI
    ATOS MEDICAL INC.·00817126020955·2010-070 Laryngectomy Pulmonary Kit with Standa...

    Santis Pre Bent Rod 5.5mmx70mm

    FDA UDI
    Lanterna Medical Technologies GmbH·07640159550617·Santis Pre Bent Rod 5.5mmx70mm

    GMA 2.0 Pedicle Screw System

    FDA UDI
    GRAFTON MEDICAL ALLIANCE, INC.·00810021380278·PRE-BENT ROD, ø5.5 X 70

    6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 70/16 mm

    FDA UDI
    mahe medical gmbh·EMAH00100100700·6.5 Cancellous Bone Shaft Screw, hex, St.Ste...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659173354·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...

    10 x 70mm Anodized SI Implant

    FDA UDI
    Osteocentric Technologies, Inc.·00810097800120·10 x 70mm Anodized SI Implant

    SANTIS™ PRE BENT ROD 5.5mm X70mm -STERILE

    FDA UDI
    Lanterna Medical Technologies GmbH·07640159551737·SANTIS™ PRE BENT ROD 5.5mm X70mm -STERILE

    Integrity-SI Fusion System

    FDA UDI
    Lincotek Medical LLC·B57112521010070D0·10 x 70 mm Anodized SI Implant

    INSET

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 26, 2025

    INSET I

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 5, 2025

    FLOCATH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RADIOMED SOURCE

    FDA 510(k)
    FDA Class 2 ·Radiology

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 18, 2025

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 22, 2025

    INSET I

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 11, 2025

    INSET I

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 18, 2025

    INSET I

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 7, 2025

    SEE H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007