BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    PULL-APART INTRODUCER (SHEATH)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867046221·DRV SFT,T15 HEXALOBE,CANN,STR

    SPECTRON PRIMARY STEM FEMORAL PROSTHES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ambu aScope 3 Slim 3.8/1.2 and Ambu aScope 4 Broncho Slim 3.8/1.2; Ambu aScope 3 Regular 5.0/2.2 and Ambu aScope 4 Broncho Regular 5.0/2.2; Ambu aScope 3 Large 5.8/2.8 and Ambu aScope 4 Broncho Large 5.8/2.8; Ambu aView Monitor

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

    DRV SFT,T15 HEXALOBE,CANN,STR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·April 18, 2022

    MENTOR SMOOTH ROUND HIGH PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·November 27, 2019

    FONAR 360

    FDA Adverse Event
    Malfunction ·FONAR CORP.·Product code LNH·February 6, 2014

    PRODISC-C IMPLANT LARGE

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·October 14, 2010

    SECURE 3 MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·November 14, 2012