BEUDAMED
    2,964 results · 33ms · Sources: EU EUDAMED, US FDA

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    Membrane Seperator

    FDA UDI
    Osstem Implant Co., Ltd.·08800000945422·

    AMICUS SEPARATOR SYSTEM/ AMICUS SEPERATOR SYSTEM;REFURBISHED

    FDA 510(k)
    FDA Unclassified ·Unknown

    Kii® Seperator Access System

    FDA UDI
    APPLIED MEDICAL RESOURCES CORPORATION·00607915123536·Laparoscopic Trocar Sleeve/Single Use

    Kii® Seperator® Dual Pack

    FDA UDI
    APPLIED MEDICAL RESOURCES CORPORATION·00607915123543·Laparoscopic Trocar Sleeve/Single Use

    ZIMMER FEMORAL SEPERATOR

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HSD·May 2, 2014

    PARFIN CUTTER/DISPENSER

    FDA Adverse Event
    Injury ·THERMO SEPERATION PRODUCTS·Product code IDW·November 20, 1994

    PROFILE GT ROTARY INSTRUMENT

    FDA Adverse Event
    Malfunction ·DENTSPLY TULSA·Product code DZA·March 22, 2006

    LIFESHIELD PRIMARY PIGGYBACK SET NV

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD./ABBOTT LTD·Product code FPA·July 26, 2004

    BD Vacutainer® Serum Seperator (SST) Blood Collection Tubes

    FDA UDI
    BECTON, DICKINSON AND COMPANY·30382903679905·TUBE SST PLC 16X125 10.0 PLBLCE RD/GR

    HI-TORQUE FLEXI-WIRE GUIDE WIRE

    FDA Adverse Event
    Injury ·GUIDANT VASCULAR INTERVENTION·Product code DQX·October 13, 2005

    PROULTRA ENDO TIPS

    FDA Adverse Event
    Malfunction ·DENTSPLY TULSA·Product code ELC·May 26, 2006

    PROULTRA

    FDA Adverse Event
    Malfunction ·DENTSPLY TULSA·Product code ELC·September 15, 2005

    PROULTRA

    FDA Adverse Event
    Malfunction ·DENTSPLY TULSA·Product code ELC·February 15, 2006

    SHILEY TRACHEOSOFT TRACHESTOMY TUBE 7.0MM.

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL·Product code JOH·July 15, 2004

    PROULTRA

    FDA Adverse Event
    Malfunction ·DENTSPLY TULSA DENTSPLY TULSA·Product code ELC·September 15, 2005

    PROFILE GT ROTARY INSTRUMENT

    FDA Adverse Event
    Malfunction ·DENTSPLY TULSA·Product code EKS·May 26, 2006

    PROULTRA

    FDA Adverse Event
    Malfunction ·DENTISPLY TULSA·Product code ELC·January 10, 2005

    ROSS LABS

    FDA Adverse Event
    Injury ·ROSS LABORATORIES·Product code FFW·March 8, 1995

    PROFILE GT ROTARY INSTRUMENT

    FDA Adverse Event
    Malfunction ·DENTSPLY TULSA·Product code EKS·May 26, 2006

    PROFILE NT ROTARY INSTRUMENT

    FDA Adverse Event
    Malfunction ·DENTSPLY TULSA·Product code DZA·June 17, 2005