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

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    DI-CROWN

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PANAVIA F

    FDA 510(k)
    FDA Class 2 ·Dental

    SMR ECCENT. GLENOSPHERE Ø 36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·September 5, 2019

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NIK·October 31, 2012

    PROMUS PREMIER?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·May 15, 2014

    ACUSNARE POLYPECTOMY SNARE

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code KNS·August 12, 2010

    Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

    FDA Enforcement
    Class II ·Terminated·TELEFLEX MEDICAL INC·August 5, 2020