BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    CORDIS BRITE TIP CATHETER SHEATH INTRODUCER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    A-GENT TRIGLYCERIDES

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    A&J POCA01 OXYGEN CONCENTRATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·January 30, 2013

    UNKNOWN DEPUY DOME SCREW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HWC·July 31, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·January 25, 2011

    VERTEBRAL BODY RETAINER

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·March 21, 2019