BEUDAMED
    49 results · 26ms · Sources: EU EUDAMED, US FDA

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    FLXfit™

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293586·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049750·Steinmann Pins, Single trocar, round end, .125-...

    Steinmann pin w. trocar/round end 3.2mm/229mm, 6 pcs./unit

    FDA UDI
    mahe medical gmbh·EMAHKM715190·Steinmann pin w. trocar/round end 3.2mm/...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659484979·Steinmann pin w. trocar/round end _x000D_...

    SR MCP

    FDA UDI
    Stryker GmbH·00886385020891·S.R. MCP METACARPAL BROACH, SIZE XL

    HEMCON CHITOFLEX-SURGICAL DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    PARIETEX PLUG AND PATCH

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

    BD VACUTAINER® SST¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·February 4, 2026

    COLON DECOMPRESSION SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FEG·November 8, 2022

    COLON DECOMPRESSION SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FEG·November 8, 2022

    COLON DECOMPRESSION SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FEG·November 8, 2022

    COLON DECOMPRESSION SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FEG·November 8, 2022

    COLON DECOMPRESSION SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FEG·November 7, 2022

    COLON DECOMPRESSION SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FEG·November 8, 2022

    COLON DECOMPRESSION SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FEG·February 15, 2022

    COLON DECOMPRESSION SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FEG·November 10, 2022

    HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code LFL·July 20, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013

    STERRAD NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·September 17, 2008