BEUDAMED
    12 results · 38ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Nd:Yag Laser Therapy Systems

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

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111355257·SKLARLITE ROCH-PEAN STR 6.25"

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668103166·GUIMARAES CORNEAL SPATULA

    TARAS THREADED FIXATION PIN

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNGO.PLAZA VB10A

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·July 22, 2018

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 19, 2018

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 15, 2018

    SPINAL CORD STIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·November 13, 2008

    VENTURE ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·September 2, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2013

    LGN PS HIGH FLEX XLPE SZ 5-6 15MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 18, 2019