BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    MULTISET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994236678·CURETTE 2940055 RVRS ANG SRTD CUP CRT

    Posicast Thermoplastic

    FDA UDI
    MEDTEC, INC.·10841439101787·Disposable non-sterile LPR55 Posicast Multiperf...

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867060203·ECLIPSE DRILLING TEMPLATE

    POLYLASE LP

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

    ENDOSKELETON(R) TL INTERBODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·February 1, 2013

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 29, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2014

    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

    FDA Enforcement
    Class II ·Terminated·Capintec Inc·April 1, 2020