BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Electrosurgical Generator ESG-200

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

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5821606390·

    HAMILTON-C6

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·October 31, 2023

    ENDOWRIST ONE VESSEL SEALER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PERFORMAX PEDIATRIC SE TOTAL FACE MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 10, 2013

    CENTRICITY RA1000

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE INTEGRATED IT SOLUTIONS·Product code LLZ·September 1, 2008

    GO BED PLUS

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 30, 2011

    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