BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    OMNISTICK

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    NA

    FDA UDI
    Richard Wolf GmbH·04055207039816·OBTURATOR FOR CANNULA OD 4.5MM WL 115mm, sharp...

    Disposable Anesthesia Circuits

    FDA UDI
    WESTMED, INC.·00709078010422·Anesthesia Circuit, Adult, 60" GSE w/Cap, Bifur...

    CERTAIN BELLATEK PROVISIONAL ABUTMENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNTHES STAINLESS STEEL MODULAR HAND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARGYLE SALEM SUMP TUBE WITH ANTI-REFLUX VALVE

    FDA Adverse Event
    Malfunction ·SHERWOOD DAVIS AND GECK·Product code KNT·August 29, 1996

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·May 23, 2014

    FILTERWIRE EZ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SAN JOSE·Product code NFA·November 13, 2012

    MD - DISPOSABLE

    FDA Adverse Event
    Malfunction ·Product code FPA·September 10, 2010

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 433170.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020