BEUDAMED
    9 results · 32ms · Sources: EU EUDAMED, US FDA

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    VK100 Percutaneous Vertebral Augmentation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Midmark

    FDA UDI
    MIDMARK CORPORATION·00841709122224·Track and Trolley Assembly used for Track Mount...

    TI PREPABLE ABUTMENT, MODEL 1618, 1619, 1620

    FDA 510(k)
    FDA Class 2 ·Dental

    SAM CHEST SEAL WITH VAVLE; SAM CHEST SEAL

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MIDWEST LOW SPEED ATTACHMENTS - CONTRA ANGLE SHEATH

    FDA Adverse Event
    Malfunction ·SIRONA DENTAL SYSTEMS GMBH·Product code EFB·April 20, 2023

    PURESOM NASAL MASK-SMALL, PURESOM NASAL MASK-MEDIUM, PURESOM NASAL MASK-LARGE, MODELS 11924-01, 11924-02, 11924-03

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ONE TOUCH FASTTAKE METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·October 15, 2008

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·July 26, 2011

    LTV

    FDA Adverse Event
    Malfunction ·CAREFUSION 203, INC.·Product code CBK·June 18, 2013