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

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    Shiley Neonatal/Pediatric Tracheostomy Tube

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583030098·ENCHANT 100 MNR T FW 1.0

    ANTARES PHARMA, INC.

    FDA registration
    ANTARES PHARMA, INC.·1 product·🇺🇸 United States

    SURGIPLUS SMS SURGICAL DRAPE (STERILE/NON-STERILE), SURGIPLUS SPP WITH PE LAMINATED SURGICAL DRAPE (STERILE/NON-STERILE)

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

    AMCO REPLACEMENT BATTERY FOR POWERHEART AED, NON-RECHARGEABLE, MODEL 2L561; G3, NON-RECHARGABLE, MODEL 7L561

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    6000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 11, 2013

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 9.75CM

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·July 8, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 17, 2014

    Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Left, Product No. LJV191T

    FDA Enforcement
    Class II ·Terminated·Integra LifeSciences Corp.·April 24, 2019