BEUDAMED
    39 results · 27ms · Sources: EU EUDAMED, US FDA

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    POWERWIRE RADIOFREQUENCY GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981216672·Trial, 31mm x 24mm x 16mm, 15 Deg

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981214692·Interbody, 31mm x 24mm x 16mm, 15 Deg

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111357572·PUMP FOR 10-1613 SKLAR KLEEN

    3D Printed Interbody System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981303440·Interbody, 31mm x 24mm x 16mm, 15 Deg, 3D

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383554305·Gutta Percha Points is used to root canal filin...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383501880·Gutta Percha Points is used to root canal filin...

    eTRAX™ Needle

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436103418·Sterile needle, 16GA x 15cm with (7.6 tapered t...

    eTRAX™ Needle

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436103404·Sterile needle, 16GA x 15cm with (7.6 tapered t...

    LEKON

    FDA UDI
    C A I INDUSTRIES CORP·00807689022015·Acupuncture needles

    NOVATEMP

    FDA UDI
    NOVAMED-USA INC.·00817499020378·10FR esophageal/rectal temperature probe/400 se...

    NA

    FDA UDI
    aap Implantate AG·04042409048838·K-wire with thread and trocar point, ø1.6, L 150

    NOVATEMP

    FDA UDI
    NOVAMED-USA INC.·00817499020064·10FR ESOPHAGEAL/RECTAL TEMPERATURE PROBE WITH 4...

    HUNTER SCIENTIFIC INJECTION PIPETTES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ARSTASIS ACCESS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    aap Implantate AG·04042409048845·K-wire with thread and trocar point, ø1.6, L 150

    ENDURO MENISCAL COMPONENT F2 10MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code KRO·January 14, 2015

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 1, 2013

    LAP-BAND SYSTEM ACCESS PORT II KIT

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·August 27, 2014

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KDJ·May 25, 2011