BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    LEGIONELLA DIFFERENTIATION DISK

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NA

    FDA UDI
    Richard Wolf GmbH·04055207043349·RECTOSCOPE-OBTURATOR Ø 14.5MM TL 327MM TL 327m...

    ZTI IMPLANTS SYSTEM, DRM IMPLANTS

    FDA 510(k)
    FDA Class 2 ·Dental

    ImagingRing m (Version 2.0); Loop-X (Version 2.0); Loop-X Mobile Imaging Robot (Version 2.0)

    FDA 510(k)
    FDA Class 2 ·Radiology

    ARTICUL/EZE BALL 28 +1.5 GR

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 27, 2014

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·November 15, 2012

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 10, 2015

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018