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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    SYNTHES COMBINATION CLAMP AND DYNAMIZATION CLIP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral HD

    FDA UDI
    Merz Dental GmbH·D7091973017·posteriors; shade A2; size S; lower jaw

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197077620·Ribbon Retractor 17 x 2...

    Kindguard Powder Free Vinyl Patient Examination Gloves, Clear (non-colored)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    STRYKER STRI-SHIELD FLYTE TOGAS

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

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024159037·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024159051·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024159044·

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 21, 2013

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 20, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·August 1, 2014

    ADJUSTABLE CERVICAL DISTRACTOR-LEFT

    FDA Adverse Event
    Malfunction ·SYNTHES TUTTLINGEN·Product code LXH·December 13, 2016