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

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    HS Fiber Sutures

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

    24M - Nevada Energy - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588011639·24M - Nevada Energy - Metal

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111148460·SKLIT XD STRABIS SCIS CVD 4.5"

    SPROTTE®

    FDA UDI
    Pajunk GmbH Medizintechnologie·04048223116524·Needle

    Intrigue

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573021277·INTRG WHISP ROTH 1BIC -17T 0A 022 LO

    SPROTTE®

    FDA UDI
    Pajunk GmbH Medizintechnologie·04048223065457·Needle

    SPROTTE® NRFit

    FDA UDI
    Pajunk GmbH Medizintechnologie·14048223027025·SPROTTE® NRFit

    Brisbane ALIF Cage

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215018238·

    Bone Cement Genta, Bone Cement HV, Bone Cement LV

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SEZ SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYNCHROMED EL

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code LKK·November 12, 2008

    8F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·August 25, 2011

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·July 17, 2013

    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V

    FDA Enforcement
    Class II ·Terminated·Roche Diagnostics Corporation·March 14, 2018