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

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    ORTHOPEDIC PACKS

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

    PHARMCHEM, INC.

    FDA registration
    PHARMCHEM, INC.·2 products·🇺🇸 United States

    DO NOT USE-NANOTITE TM CERTAIN¿ IMPLANT 4 X 15MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·September 18, 2024

    DO NOT USE-NANOTITE TM CERTAIN¿ IMPLANT 4 X 15MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·September 18, 2024

    ViewFlex™ X ICE Catheter, Sensor Enabled™

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERIFYNOW-P2Y12 ASSAY

    FDA 510(k)
    FDA Class 2 ·Hematology

    JUGGERSTITCH CURVED IMPLANT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·February 13, 2025

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 8, 2013

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·December 13, 2010

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 22, 2014