BEUDAMED
    28 results · 24ms · Sources: EU EUDAMED, US FDA

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    OSSTEM Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    X-CORE

    FDA UDI
    Nuvasive, Inc.·00887517244062·X-CORE 2 Ti Endcap, 16mm Rnd 4° Ø16

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528102084·3.1 mm Cannulated Drill, Standard AO Quick Release

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694043298·1.6mm X 4mm Screw

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528108222·3.1 mm Cannulated Drill, Standard AO Quick Rele...

    VSI MICRO-INTRODUCER SETS (REGULAR, STIFFEN), MODELS 7197V-7209V, 7240V-7256V, 7259V, 7230V, 7231V, 7260V, 7274V

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LANO-E

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 14, 2017

    COOK TURBO-FLO HD HEMODIALYSIS CATHETER TRAY

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MPB·December 19, 2016

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 8, 2017

    ENDOPATH XCEL BLUNT TIP TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·June 11, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 14, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·September 12, 2008

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 10, 2017

    ATTUNE FB TIB BASE SZ 7 POR

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 3015516266·Product code MBH·November 4, 2025

    UNK ATTUNE KNEE PATELLA

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·November 4, 2025

    COOK TURBO-FLO HD HEMODIALYSIS CATHETER TRAY

    FDA Adverse Event
    Injury ·COOK INC·Product code MPB·August 1, 2018

    COOK TURBO-FLO HD HEMODIALYSIS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code MPB·June 13, 2017

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022