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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ENTERIX INSUREFIT FOB CONTROLS, MODEL 16800

    FDA 510(k)
    FDA Class 2 ·Hematology

    Endeavour™ TruColor™

    FDA UDI
    METREX RESEARCH, LLC·00810210820240·Endeavour™ TruColor™ headlight system - North A...

    Vascular Silicones Ties, Extra Mini Blue, sterile

    FDA UDI
    Batrik Medical Manufacturing Inc·00690521022270·Vascular Silicone Ties, Radio Opaque, Sterile, ...

    Forceps, Surgical, acc. Adson 12.0cm 1x2 mouse-teeth behind serrated

    FDA UDI
    Geister Medizintechnik GmbH·04057034021620·Forceps, Surgical, acc. Adson 12.0cm...

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365121333·

    MODIFICATION TO PLEURX PLEURAL CATHETER AND DRAINAGE KITS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEEDLELESS TRANSFER DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Widex

    FDA UDI
    Widex A/S·05706069722390·Widex D-PA BTE (Titan grey S-220 ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069722697·Widex CLEAR220 C2-FS BTE (Titan grey S-220 ) Te...

    Widex

    FDA UDI
    Widex A/S·05706069720884·Widex UNIQUE U-PA BTE (Titan grey S-220 ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069721973·Widex D-FS BTE (Titan grey S-220 ) Telecoil, RC...

    Widex

    FDA UDI
    Widex A/S·05706069721652·Widex UNIQUE U-FS BTE (Titan grey S-220 ) Telec...

    Widex

    FDA UDI
    Widex A/S·05706069721164·Widex BEYOND B-F2 (Titan grey S-220 ) Telecoil,...

    H5I- ROW

    FDA Adverse Event
    Malfunction ·RESMED LTD.·Product code BZD·May 1, 2013

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 7, 2008

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 10, 2011

    THROMBUSTER II

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code MMY·March 17, 2014

    THROMBUSTER II

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code DXE·October 23, 2012

    THROMBUSTER II

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code DXE·December 21, 2012

    THROMBUSTER II

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code DXE·January 16, 2019