BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    KOWA HAND-HELD APPLANATION TONOMETER HA-1

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Amendia Interbody Fusion Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JSZ MULTIACTION GP CONTACT LENS SOLUTION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ENDOPATH ENDOSCOPIC VASCULAR LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 12, 1996

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 30, 2013

    S-ROM SLEEVE PRX ZTT, 20D-LRD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, DEPUY-CORK·Product code MRA·January 11, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 28, 2014

    Heritage Labs Appraise A1c Diabetes Home Test , Product K7609, 24 kits/shipping carton (Product K7609), each kit packed in a box and contains 1 Triad Medium Alcohol Prep Pad, Cat. No. 10-3001, NDC 50730-3001-0, and blood specimen collection supplies, forms, and instructions Blood specimen collection

    FDA Recall
    Terminated ·Heritage Labs International LLC·Product code LCP·January 9, 2011