BEUDAMED
    1,703 results · 24ms · Sources: EU EUDAMED, US FDA

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    MR Q; MR Q SUPINE; MR Q SLT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749045413·CERAMO HCR valve forceps 3.0 x 15/350 mm, with ...

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749045444·CERAMO HCR forceps russian model, 350 mm

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749045406·CERAMO HCR knot pusher 25° angl., 280 mm

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749045390·CERAMO HCR nerv hook 1 x 7 / 280 mm

    MR Q

    FDA UDI
    Meridian Medical d.o.o.·03830074980017·The MR Q is a Q-switched Nd:YAG ophthalmic lase...

    ScanDiags Ortho L-Spine MR-Q

    FDA 510(k)
    FDA Class 2 ·Radiology

    MR Q supine

    FDA UDI
    Meridian Medical d.o.o.·03830074980000·The MR Q supine is a Q-switched Nd:YAG ophthalm...

    MR Q SLT

    FDA UDI
    Meridian Medical d.o.o.·03830074980024·The MR Q SLT is a Q-switched Nd:YAG ophthalmic ...

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·December 15, 2016

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code OGE·July 17, 2018

    EPIDURAL CATHETERIZATION SET: 19 GA

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·August 17, 2016

    EPIDURAL CATHETERIZATION COMPONENT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·April 3, 2018

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·May 10, 2016

    EPIDURAL CATHETERIZATION KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·April 11, 2017

    EPIDURAL CATHETERIZATION KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·April 11, 2017

    Cell Marque, PAX8 (MRQ-50 Mab.), 7 mL, REF PA0808, IVD, This antibody is intended for in vitro diagnostic (IVD) use. PAX-8 (MRQ-50) Mouse Monoclonal Primary Antibody is intended for laboratory use in the detection of the PAX-8 protein in formalin-fixed, paraffin-embedded tissue stained in qualitative immunohistochemistry (IHC) testing

    FDA Enforcement
    Class II ·Terminated·Leica Biosystems Richmond Inc.·September 20, 2017

    MUM1 (MRQ-43) Rabbit Monoclonal Antibody

    FDA UDI
    CELL MARQUE CORPORATION·00841683113638·

    CD56 (MRQ-42) Rabbit Monoclonal Antibody

    FDA UDI
    CELL MARQUE CORPORATION·00841683120186·

    CD3 (MRQ-39) Rabbit Monoclonal Antibody

    FDA UDI
    CELL MARQUE CORPORATION·00841683123170·