BEUDAMED
    13 results · 23ms · Sources: EU EUDAMED, US FDA

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    TEVADAPTOR; CONNECTING SET W/ ULTRASITE INJECTION SITE, SPIKE PORT ADAPTOR SET W/ ULTRASITE INJECTION SITE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221037152·Unitek(TM) Bicuspid Band General Purpose Wide U...

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515018402·Roch-Pean Hemo Fcps, str, 8"

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321413060·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311413060·

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857580817·Split Tube Retractor Ø20x80 mm

    NUMED PTS X SIZING BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SP DYNAMIS, SP SPECTRO, XS DYNAMIS, XS SPECTRO, XP DYNAMIS, XP SPECTRO, MODELS M021-4AF/3, M002-2A

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    INTIMA-II 20GAX1.16IN PRN SLM

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·January 14, 2020

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MPRI·Product code DTB·June 3, 2013

    LCS DD ROT BRG LG 10.0MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·June 22, 2011

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 3, 2008

    Disetronic D-TRONplus Insulin Pump Battery Pack; Ref/Catalog no. 04697014001.

    FDA Recall
    Terminated ·Disetronic Medical Systems, Inc.·Product code LZG·July 13, 2006