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

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    Filters Regulation: Us FDA ×

    Reprocessed Webster Duo-Decapolar Diagnostic EP Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HD ENDOEYE, MODELS WA50011A, WA50013A, WA50013L, WA50013T, WA50015L

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

    INVADER FACTOR V

    FDA 510(k)
    FDA Class 2 ·Hematology

    CUI TEXTURED SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·October 2, 2019

    TRULIANT TIB IMP CRC INSERT SZ 5, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 1, 2024

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·July 19, 2011

    GUT SURGICAL SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAL·June 26, 2013

    6.0MM COLLAR FOR TRANS-CONNECTOR CLAMP

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code NKB·October 21, 2014

    PAEDIATRIC CANNULA, VENOUS

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DWF·June 7, 2023