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

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    TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TURBO-JECT® DOUBLE LUMEN POWER-INJECTABLE PICC

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·December 3, 2015

    HOFFMANN II EXTERNAL FIXATION SYSTEM LINE EXTENSION MODEL 4920-1-010, 4920-1-020, 4920-1-030, 4920-1-100, HOFFMANN II EX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VIDAPORT INTRAOSSEOUS INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AEQUALIS REVERSED BASE PLATE TA6V LONG PEG WITH HA

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·April 19, 2023

    LOGIC CR TIB INSERT STD, SZ 1.5, 9 MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 28, 2024

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 1, 2014

    EDS III CSF DRAIN SYS W/O V CATH

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·May 29, 2013

    FOX PLUS PTA CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LIT·June 17, 2011

    Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator

    FDA Enforcement
    Class II ·Ongoing·Abbott·November 8, 2023