BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    GENESIS UNICOMPARTMENTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HSX·October 15, 2025

    GENESIS UNI KNEE FEMORAL COMPONENT COCR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HSX·May 23, 2025

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909127352·REVELATION DIAMOND 855-012SC - 5 PACK

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110874·TIP GUARDS VENTED GREEN PACK OF 100

    TAMARIN BLUE PTCA RX DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLEARFIL DC CEMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    EQUINOXE REPLICATOR PLATE 4.5MM O/S

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·December 20, 2022

    SYMBIQ DUAL CHANNEL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 14, 2014

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 2, 2010

    REACH TOTAL CARE PLUS WHITEN TOOTHBRUSH USA

    FDA Adverse Event
    Malfunction ·SKILLMAN CONTRACT·Product code EFW·January 14, 2013