BEUDAMED
    28 results · 29ms · Sources: EU EUDAMED, US FDA

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    ARK METHOTREXATE ASSAY, ARK METHOTREXATE CALIBRATOR, ARK METHOTREXATE CONTROL, ARK METHOTREXATE CONTROL (CALIBRATION RAN

    FDA 510(k)
    FDA Unclassified ·Unknown

    Arm Rest Breast

    FDA UDI
    Noras MRI products GmbH·04251269200366·

    MAXCUT CARBIDE BUR (100/pk) FG 1/2

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77811119041·MAXCUT CARBIDE BUR (100/pk) Shape: Round; Size:...

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00850038691042·

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190400070·7mm LG Adjustable HL Implant, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190400120·12mm LG Adjustable HL Implant, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190400110·11mm LG Adjustable HL Implant, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190400130·13mm LG Adjustable HL Implant, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190400100·10mm LG Adjustable HL Implant, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190400140·14mm LG Adjustable HL Implant, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190400080·8mm LG Adjustable HL Implant, HiJAK™ Cervical

    Surgical Direct

    FDA UDI
    Surgical Direct, Inc.·B382SD221081119040·10 3/4" Malis Bayonet Bipolar Forceps with Irri...

    NEXGEN PRIMARY POROUS PATELLA, MODEL 04-211-IIII-5878-65-ZZ-(STANDARD),04-212-IIII-5878-61-ZZ-(MICRO)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMARTXIDE 50 HS/MS

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

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190400090·9mm LG Adjustable HL Implant, HiJAK™ Cervical

    INCLUSIVE TAPERED IMPLANT 3.7 MMD X 8 MML X 3.5 MMP

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·July 1, 2023

    INCLUSIVE TAPERED IMPLANT 3.7 MMD X 8 MML X 3.5 MMP

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·July 5, 2023

    VITEK® 2 AST-ST01 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·October 24, 2017

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 14, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·August 12, 2008