BEUDAMED
    40 results · 22ms · Sources: EU EUDAMED, US FDA

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    RANDOX CALCIUM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040179444·Diamond Discs

    TEWA

    FDA UDI
    asia-med GmbH·04251282508111·TeWa CB-Type 2513: coated acupuncture needles ...

    TEWA

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282500795·TeWa CB-Type 2513: coated acupuncture needles ...

    NeuroNav Headstage cable

    FDA UDI
    ALPHA OMEGA ENGINEERING CO. LTD.·07290114061339·

    NeuroNav Headstage cable

    FDA UDI
    ALPHA OMEGA ENGINEERING CO. LTD.·07290114063678·

    DATEX-OHMEDA TEC 6 PLUS ANESTHESIA VAPORIZER, DATEX-OHMEDA TEC 6 PLUS NAD VARIANT ANESTHESIA

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HARDYDISK TICARILLIN 75MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    STERLING¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·March 12, 2013

    SMART CONTROL NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIO·February 24, 2011

    ICY HOT HEAT THERAPY AIR

    FDA Adverse Event
    Injury ·*·Product code IMD·February 20, 2008

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 11, 2019

    UNKNOWN HIP IMPLANT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 8, 2019

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·November 11, 2019

    Bard Access Systems, Inc., Gauderer Genie* II PEG (Percutaneous Endoscopic Gastrostomy) Safety System Guidewire Placement Technique REF 000375, 20F, STERILE.

    FDA Recall
    Terminated ·C.R. Bard Access Systems, Inc·Product code KNT·December 4, 2008

    OES CYSTONEPHROFIBERSCOPE

    FDA Adverse Event
    Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FAJ·August 23, 2024

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·November 8, 2019

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 27, 2019

    UNKNOWN HIP ACETABULAR LINERS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 8, 2019

    UNKNOWN HIP ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 8, 2019