BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    Phototherapy System

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

    FLOW CONTROLLER

    FDA 510(k)
    FDA Unclassified ·Unknown

    THE PL-1064 LASER SYSTEM

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

    ULTRAPRO HERNIA SYSTEM UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·February 20, 2021

    LIGAMAX - 5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code FZP·October 9, 2008

    REFLEX HYBRID REVISION DRIVER DRAW ROD SCREW EXTRA

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code LXH·July 19, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 26, 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