BEUDAMED
    33 results · 21ms · Sources: EU EUDAMED, US FDA

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    CHARLOTTE HIGH-DEMAND COMPRESSION SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Natus

    FDA UDI
    NATUS NEUROLOGY INCORPORATED·00382830063272·EMG USB Control Panel II

    LACTOSORB RAPIDFLAP

    FDA 510(k)
    FDA Class 2 ·Dental

    VERSALAB APM

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

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119431·TLIF, 28mm X 10mm X 11mm, Convex 5°, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119448·TLIF, 28mm X 10mm X 12mm, Convex 5°, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119394·TLIF, 28mm X 10mm X 7mm, Convex 5°, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119400·TLIF, 28mm X 10mm X 8mm, Convex 5°, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119479·TLIF, 28mm X 10mm X 15mm, Convex 5°, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119417·TLIF, 28mm X 10mm X 9mm, Convex 5°, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119462·TLIF, 28mm X 10mm X 14mm, Convex 5°, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119424·TLIF, 28mm X 10mm X 10mm, Convex 5°, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119455·TLIF, 28mm X 10mm X 13mm, Convex 5°, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523119486·TLIF, 28mm X 10mm X 16mm, Convex 5°, T3

    LINEAR 7.5 FR. 25CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 17, 2019

    LINEAR 7.5 FR. 25CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 17, 2019

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·April 9, 2013

    UNIVERSAL DRILL GUIDE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·February 25, 2011

    CONTAK RENEWAL 3

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008

    ZILVER 635 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·May 25, 2011