BEUDAMED
    10 results · 21ms · 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 ×

    BIVONA CUSTOMIZED TRACHEOSTOMY TUBES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PREVENA INCISION MANAGEMENT SYSTEM WITH CUSTOMIZABLE DRESSING

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

    GUARDWIRE TEMPORARY OCCLUSION AND ASPIRATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LATERAL STRAIGHT STEM 15.0 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·March 28, 2012

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 22, 2013

    BREEZE2

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·December 8, 2010

    VICTORY XL DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 9, 2014

    SULOX-HD 32 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·April 23, 2019

    SULOX, HEAD, M¸ 32/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·August 3, 2018

    SULOX-HEAD 28 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·April 4, 2019