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

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    ARTHROCARE HEAD AND NECK COBLATION WAND

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772813858·GENUMEDI PRO SILVER SIZE V

    Trivicta

    FDA UDI
    Ortho Development Corporation·00822409123834·Collar EXT Size 5

    COE-FLEX®

    FDA UDI
    Gc America Inc.·D6581312051·COE-FLEX® s Regular Body, Fast Set (base only) ...

    COE-FLEX®

    FDA UDI
    Gc America Inc.·10386040004916·COE-FLEX® s Regular Body, Fast Set (base only) ...

    N/A

    FDA UDI
    TETRA MEDICAL SUPPLY CORP.·00614138221871·NEOPRENE PATELLAR KNEE SUPPORT, XXLARGE

    OneLIF™

    FDA UDI
    Novapproach Spine LLC·G07001131312050·Trial-OneLIF Interbody, Large, 13 Degree, 12mm ...

    OneLIF™

    FDA UDI
    Novapproach Spine LLC·G07001031312050·OneLIF Interbody, Large, 13 Degree, 12mm X 5mm

    MICROSCAN (R) MICROSTREP PLUS (R) PANELS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PASCO MIC AND MIC/ID PANELS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    COOK® CERVICAL RIPENING BALLOON

    FDA Adverse Event
    Malfunction ·COOK INC·Product code PFJ·July 18, 2016

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005248·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005279·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005262·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005255·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005286·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005293·CONTINUOUS SUCTION REGULATORS

    COOK® CERVICAL RIPENING BALLOON

    FDA Adverse Event
    Malfunction ·COOK INC·Product code PFJ·July 19, 2016

    ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·February 3, 2017

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·May 23, 2013