BEUDAMED
    1,277 results · 22ms · Sources: EU EUDAMED, US FDA

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    Bronchoscope System, The Single-use Bronchoscope (Single-use Bronchoscope: SP-Y-ZQGJ2.8, SP-Y-ZQGJ3.8, SP-Y-ZQGJ4.2, SP-Y-ZQGJ4.8, SP-Y-ZQGJ5.2, SP-Y-ZQGJ5.8; Electronic Endoscope Imaging Processor: SP-TXCLQ12.1)

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ARKEO, Wedge Fixation System

    FDA UDI
    Auxano Medical LLC·00850055649934·ARKEO Evan's Wedge Trial, 20x20x10

    Introcan Safety ® 2

    FDA UDI
    B. BRAUN MEDICAL INC.·04046955746101·Introcan Safety® 2 IV Catheter - 20 Ga. x 2.0 in.

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809763503085·Long Tab Protector

    Perfect Fit

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377022029·Interface Cable, FastTrack, Abdomen, Alice 5

    Symmetry Charnley

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482061121·Symmetry® Retractor, Charnley Blade, Long Round...

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981247614·No-Profile Interbody, 43mm x 30mm x 20mm, 10 Deg

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780160236·Integra® Miltex® DeBakey Occlusion Clamp, 10", ...

    NA

    FDA UDI
    STRYKER CORPORATION·07613327056303·Mini Small-Joint Punch

    NA

    FDA UDI
    STRYKER CORPORATION·07613327056310·Mini Small-Joint Scissors

    NA

    FDA UDI
    STRYKER CORPORATION·07613327056327·Mini Small-Joint Grasper

    Disposable Vinyl Glove

    FDA 510(k)
    FDA Class 1 ·General Hospital

    POWER SCOOTER, MODEL TL-688

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962114759·CHARNLEY RETRACTOR BLADE, LONG RND, 1"X4" DEEP ...

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·March 5, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·March 5, 2010

    OPTI-FREE UNSPECIFIED PRODUCT

    FDA Adverse Event
    Injury ·ALCON - FORT WORTH / ALCON LABORATORIES, INC.·Product code LPN·March 12, 2010