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

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    SPINAL USA CEMENT RESTRICTOR SYSTEM

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

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306801426·Adson Tissue Forceps - 1x2 Teeth, Straight, 2.0...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450046470·

    PHILOS DR ACC

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO·Product code DXY·July 17, 2006

    Logical Lateralised 20° Hooded Liner

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215095307·

    KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4

    FDA 510(k)
    FDA Class 2 ·Dental

    ALLERGEN IMMUNOCAP, MODELS C74, E89, EX2, EX70, EX71, EX73, FX8, FX9, FX10, FX16, FX73, I72, I75, I76, K71, K73, K81, K8

    FDA 510(k)
    FDA Class 2 ·Immunology

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·February 26, 2018

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 20, 2013

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 17, 2008

    DISCOVERY II

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·April 15, 2011