BEUDAMED
    627 results · 29ms · Sources: EU EUDAMED, US FDA

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    MTS Ampicillin-Sulbactam 0.016/0.008 - 256/128 µg/mL

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517639479·CoRoent Ant TLIF PEEK, 9x12x34mm 15°

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169595583·TRIAL 2192345 O25 IB 27MM 12 DEG 12X45

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111093·SILICONE MAT FOR K 9-2340

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970508·

    DISTAL VOLAR RADIUS PLATING SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EASYMAX T1 SELF MONITORING BLOOD GLUCOSE SYSTEM, MODEL EPS10042

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code NIK·January 11, 2014

    2.7MM TI VA LCKNG SCR SLF-TPNGWITH T8 STARDRIVE RECESS 26MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·June 27, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 4, 2011

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 13, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·February 22, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·July 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·July 31, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 10, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 20, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·July 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·July 31, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 25, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·March 3, 2022