BEUDAMED
    77 results · 31ms · Sources: EU EUDAMED, US FDA

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    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 1S & 1P

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 1S & 1P

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·ZIRCONIA SILICATE BEAD IOL TUMBLE POLISHING

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·IRIDOCAPSULAR INTRAOCULAR LENS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 1S & 1P

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 1S & 1P

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·ZIRCONIA SILICATE BEAD IOL TUMBLE POLISHING

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·IRIDOCAPSULAR INTRAOCULAR LENS

    BaseVac

    FDA UDI
    R. E. Morrison Equipment Inc·D13028000490·2SUR4.25-1 | 9 User Dual Surgical Vacuum | NFPA...

    70 Brain Microdialysis Catheter 60/10, 4/pkg

    FDA UDI
    M DIALYSIS INC.·07332699000911·Microdialysis catheter (20 kDa cut-off, 60 mm s...

    ACUMED

    FDA UDI
    Acumed LLC·10806378039553·Radiolucent VDR Tgt Guide Assy Wide, L

    DELTA TEST AMYLASE UV

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LOCK

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LPH·September 26, 2024

    Implant, Anti-Gastroesophageal Reflux

    FDA Pre-Market Approval
    FDA Class 3 ·LINX REFLUX MANAGEMENT SYSTEM

    Transcatheter Septal Occluder

    FDA Pre-Market Approval
    FDA Class 3 ·CARDIOSEAL SEPTAL OCCLUSION SYSTEM WITH QWIKLOAD

    DURALENS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·May 4, 2016

    PINNACLE SECTOR II CUP 50MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·May 8, 2014

    MERIT CUSTOM KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code FMF·October 17, 2012

    C-ARM

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD. (GE PRIVATE)·Product code JAA·August 11, 2010

    Transcatheter Septal Occluder

    FDA Pre-Market Approval
    FDA Class 3 ·CARDIOSEAL