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

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    CRYOBALLOON ABLATION SYSTEM

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

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B58201018250·FORCEPS

    Axiom®

    FDA UDI
    AXIOM MEDICAL, INCORPORATED·M6651018250·Penrose Tubing, Silicone

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981216702·Trial, 31mm x 24mm x 18mm, 25 deg

    3D Printed Interbody System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981303464·Interbody, 31mm x 24mm x 18mm, 25 Deg, 3D

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981214722·Interbody, 31mm x 24mm x 18mm, 25 deg

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450265550·

    STANDARD IMAGING HDR 1000 PLUS ION CHAMBER; STANDARD IMAGING IVB 1000 ION CHAMBER

    FDA 510(k)
    FDA Class 2 ·Radiology

    RECTOSIGHT RS300-04;AND PROTOSIGHT PS300-04 DEVICE

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

    WAVEWRITER ALPHA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 8, 2026

    STELLARIS VISION ENHANCEMENT SYSTEM

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQC·February 5, 2026

    Widex

    FDA UDI
    Widex A/S·05706069721911·Widex D-FS BTE (Cappuccino brown S-440 ) Teleco...

    Widex

    FDA UDI
    Widex A/S·05706069721102·Widex BEYOND B-F2 (Cappuccino brown S-440 ) Tel...

    Widex

    FDA UDI
    Widex A/S·05706069722642·Widex CLEAR440 C4-FS BTE (Cappuccino brown S-44...

    Widex

    FDA UDI
    Widex A/S·05706069721591·Widex UNIQUE U-FS BTE (Cappuccino brown S-440 )...

    Widex

    FDA UDI
    Widex A/S·05706069720822·Widex UNIQUE U-PA BTE (Cappuccino brown S-440 )...

    Widex

    FDA UDI
    Widex A/S·05706069726916·Widex EVOKE E-PA (Cappuccino brown S-440 ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069722338·Widex D-PA BTE (Cappuccino brown S-440 ) RC coil

    HOMEPUMP C-SERIES, 100 ML, 2 ML/HR (CONTAINS DEHP)

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code MEB·July 7, 2021

    PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 3, 2013