BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    DENTAL CONNECTOR PRECISION ATTACHMENT

    FDA 510(k)
    FDA Class 1 ·Dental

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909124352·REVELATION DIAMOND 847KR-016M - 5 PACK

    Gen. Acces/ Instr. Tip Guard

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

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110881·TIP GUARDS VENTED RED PACK OF 100

    ENTRY SITE ALIGNMENT SYSTEM MODEL # CX9626

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    RHYTHMLINK MONOPOLAR STIMULATING INSTRUMENT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CUSA EXCEL 23KHZ STRAIGHT HANDPIECE

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES (IRELAND) LIMITED·Product code LFL·May 14, 2014

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 12, 2013

    BV 25

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZL·November 10, 2010

    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