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

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    AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEVACHECK

    FDA 510(k)
    FDA Class 2 ·Radiology

    DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE)

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

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 15, 2013

    PUMP MMT-715LNAB PRDGM INS V2.1 BL EN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code LZG·December 23, 2010

    CORAIL2 NON COL HO SIZE 9

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWY·July 29, 2014

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 433165.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020