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

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    ACTIBAND

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PERMITE

    FDA UDI
    SDI LIMITED·09336472001087·PERMITE 2SP SLOW 500

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496022404·WONDER MODEL 140 OPAQUE, SIZE XXL, NERO, GRADUA...

    nSpire Health

    FDA UDI
    NSPIRE HEALTH, INC.·10852417003672·KoKo Standard Pulmonary Function Filter, White ...

    PERMITE

    FDA UDI
    SDI LIMITED·DO3640224042·

    Cardiovascular Procedure Kit

    FDA UDI
    Terumo Cardiovascular Systems Corporation·00699753461345·

    DELTA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·34546540337543·DELTA 2.2X4MM SCREW, 4 EA

    K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MICRO-MAX, MODEL 319

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAPNOCHECK BCI Airway Adapter; Model Number BSR; Product Code WW8214

    FDA Enforcement
    Class II ·Ongoing·Smiths Medical ASD, Inc.·March 26, 2025

    MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·April 6, 2022

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·March 27, 2013

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·February 16, 2011

    EMBRACE PUMP

    FDA Adverse Event
    Malfunction ·Product code LZH·March 26, 2008

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code MNL·October 1, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code MNL·October 1, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code MNL·October 1, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code MNL·October 1, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code MNL·October 1, 2024

    FlexTray Procedure Delivery System Endopath Gynecololgy Tray, Product #FN065.

    FDA Recall
    Terminated ·Ethicon Endo-Surgery·Product code HET·November 25, 2003