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

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    SECOND GENERATION KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Lady-Comp

    FDA UDI
    Valley Electronics AG·07629999894334·

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867052413·AIM GD LT,LOCK DISTAL FIBULA PLT

    VIVALITH II 301 PULSE GENERATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MEDAID DUAL CHANNEL TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    FAST-CATH¿ HEMOSTASIS INTRODUCER, CATH-LOCK¿ LOCKING HUB, 12 CM SHEATH, 8.5 F

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code DYB·January 22, 2024

    PLUM XLM W/DATAPORT

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 23, 2014

    ARCHITECT HAVAB IGM REAGENT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INT'L, LTD·Product code LOL·November 9, 2010

    HEARTSTART MRX- EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 16, 2012