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

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    EXETER ALL PLASTIC ACETABULAR COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981202941·Interbody, 9mm x 36mm x 13mm, 20 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981194956·Interbody, 9mm x 36mm x 13mm, 20 deg

    SeaSpine Spacer System - Redondo™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981045197·Redondo Trial 26mm x 24mm x 22mm, Lordotic

    ROYAL SHIELD SHIELD GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LEEP AND LLETZ ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ASR TAP SLV ADAP 11/13 +3

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·January 30, 2013

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·December 13, 2010

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·July 15, 2014

    TFN-ADVANCED Proximal Femoral Nailing System (TFNA); for treatment of fractures in orthopedics and trauma.

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·May 20, 2015