BEUDAMED
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    ALTUS SPINE PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517565259·CoRoent Ant TLIF PEEK, 13x12x28mm 0°

    RC Multi-base Abutment

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600306337·

    HHM

    FDA UDI
    Oticon A/S·05707131256638·H150, MINIBTE 312 WL 85 TC HHM

    SUNRISE MACHINE AND TOOL, INC.

    FDA registration
    SUNRISE MACHINE AND TOOL, INC.·2 products·🇺🇸 United States

    SIREMOBIL ISO-C 3D

    FDA 510(k)
    FDA Class 2 ·Radiology

    STRAUMANN CARES SCREW-RETAINED BRIDGE TITANIUM, STRAUMANN CARES DOLDER BAR TITANIUM

    FDA 510(k)
    FDA Class 2 ·Dental

    2132280-1999-00001

    FDA Adverse Event
    Injury ·Product code FSA·April 16, 1999

    2132280-2006-00005

    FDA Adverse Event
    Death ·Product code FNG·January 23, 2007

    2132280-2005-00008

    FDA Adverse Event
    Injury ·Product code ---·October 4, 2005

    2132280-2001-00002

    FDA Adverse Event
    Product code FSA·January 31, 2001

    2132280-2001-00003

    FDA Adverse Event
    Injury ·Product code ---·May 15, 2001

    2132280-2002-00001

    FDA Adverse Event
    Injury ·Product code FSA·June 19, 2002

    2132280-1998-00001

    FDA Adverse Event
    Injury ·Product code FSA·October 7, 1998

    2132280-2001-00004

    FDA Adverse Event
    Injury ·Product code FSA·September 19, 2001

    2132280-2002-00003

    FDA Adverse Event
    Malfunction ·Product code ---·October 22, 2002

    AEQUALIS REVERSED BASE PLATE TA6V LONG PEG WITH HA

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·April 19, 2023

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 1, 2013

    RELION MICRO BLOOD GLUCOSE SYSTEM

    FDA Adverse Event
    Injury ·ARKRAY, INC.·Product code CGA·June 17, 2011