BEUDAMED
    442 results · 23ms · Sources: EU EUDAMED, US FDA

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    Agent, Bulking, Injectable For Gastro-Urology Use

    FDA Pre-Market Approval
    FDA Class 3 ·URYX URETHRAL BULKING AGENT

    Agent, Bulking, Injectable For Gastro-Urology Use

    FDA Pre-Market Approval
    FDA Class 3 ·BARD TEGRESS URETHRAL IMPLANT

    Agent, Bulking, Injectable For Gastro-Urology Use

    FDA Pre-Market Approval
    FDA Class 3 ·TEGRESS URETHRAL IMPLANT

    Agent, Bulking, Injectable For Gastro-Urology Use

    FDA Pre-Market Approval
    FDA Class 3 ·BARD TEGRESS URETHRAL IMPLANT

    Agent, Bulking, Injectable For Gastro-Urology Use

    FDA Pre-Market Approval
    FDA Class 3 ·BARD TEGRESS URETHRAL IMPLANT

    BARD TEGRESS URETHRAL BULKING AGENT

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code LNM·December 27, 2006

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950008810·ACE EXTENSION TUBE 30" STER 4CC VOLUME L/F 100/CA

    Latitude™ EV

    FDA UDI
    TORNIER, INC.·00846832002504·Ulnar Stem - Coated

    Armstrong Activent®

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490030298·VENT TUBE 1030030 5PK ARMSTR BEV GROMMET

    Invotec Silicone Sheeting

    FDA UDI
    INVOTEC INTERNATIONAL, INC.·00818501021260·Invotec Silicone Sheeting 12 x 12 x 0.030"

    Bone Screws

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132134009·STD AO DETAIL PRINT

    SCFE Screw

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132114148·4.0mm X 30mm MED THREAD CANNULATED SCREW

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420300300·Anterio Lateral Closing Wedge Osteotomy Guide, ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2711000300300·Left CHAMP Midfoot Charcot Guide, 30mm x 30mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410300300·Anterior Closing Wedge Osteotomy Guide, 30mm x ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2711010300300·Right CHAMP Midfoot Charcot Guide, 30mm x 30mm

    SIMILAR DEVICE BNI75TCDDH, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·October 2, 2017

    SIMILAR DEVICE DI7TCBLRT, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·February 9, 2015

    TI COLLAR WITH GROOVES

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MNH·April 2, 2013

    CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code DYE·March 25, 2011