BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    DeGen Navigated Instrumentation

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814749·GENUMEDI EXTRA WIDE SAND SIZE VI

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114124·CHARLEUS CORTEX EXTR 23GA 16MM PK/10

    UltraStick - HJ & Associates PL

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·00092237900901·2"x 2" Foam

    UltraStick

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·00850689007544·2"x 2" Foam

    UltraStick

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·10850689007541·2"x 2" Foam, Case of 10

    DEPUY

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295084327·DEPUY TRIAL TAPER SPACER -3 12/14 TAPER

    CANON FULL AUTO TONOMETER TX-F

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ARTHREX TITANIUM CORKSCREW, 3.5 MM, ARTHREX TITANIUM CORKSCREW, 5.0 MM, ARTHREX TITANIUM CORKSCREW 6.5MM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALEUTIAN Interbody Systems

    FDA UDI
    VB Spine LLC·10888857188365·Parallel Angled Trial Size 18x60x14 mm

    TRIAL SPACER 12/14 +0

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code LXH·May 18, 2018

    TRIAL SPACER 12/14 -3

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·May 18, 2018

    TRIAL SPACER 12/14 +5

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·May 18, 2018

    TRIAL SPACER 12/14 -3

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·May 18, 2018

    TRIAL SPACER 12/14 +0

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·May 18, 2018

    TRIAL SPACER 12/14 +5

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·May 18, 2018

    TRIAL SPACER 12/14 +5

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·May 18, 2018

    TRIAL SPACER 12/14 -3

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·May 18, 2018

    TRIAL SPACER 12/14 +0

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code LXH·May 18, 2018

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·August 11, 2011