BEUDAMED
    34 results · 19ms · 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.

    DEXTROLYTE II, PERITONEAL DIALYSIS CYCLER SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SYNCARDIA FREEDOM DRIVER

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, LLC·Product code LOZ·October 21, 2019

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950022694·SUCTION TIP OPENING 3MM 7" 18CM

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377067715·RELINE C Cross Conn, 35 45mm Crossbar

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746094194·DB BRACKET MASTER SERIES MAND RIGHT/LEFT 2ND BI...

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746097041·DB BKT MASTER IBD LL CUSP 018 T-11 A+7 R=0

    SYNCARDIA FREEDOM DRIVER

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, LLC·Product code LOZ·June 15, 2021

    SYNCARDIA FREEDOM DRIVER

    FDA Adverse Event
    Injury ·SYNCARDIA SYSTEMS, LLC·Product code LOZ·April 25, 2018

    SYNCARDIA 70CC TAH-T

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, LLC·Product code LOZ·February 9, 2018

    SYNCARDIA FREEDOM AC POWER SUPPLY

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, INC.·Product code LOZ·May 3, 2016

    SYNCARDIA FREEDOM AC POWER SUPPLY

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, INC.·Product code LOZ·April 8, 2016

    SYNCARDIA FREEDOM AC POWER SUPPLY

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, INC.·Product code LOZ·November 17, 2015

    Bone wire in coils of 10m,1.2mm

    FDA UDI
    mahe medical gmbh·EMAH00409000120·Bone wire in coils of 10m,1.2mm

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659210332·Bone wire in coils of 10m,1.2mm _x000D_...

    900-012 Extended Malar Sizer Set

    FDA UDI
    IMPLANTECH ASSOCIATES, INC.·M7249000121·Malar Sizer Set

    Stryker F1

    FDA UDI
    STRYKER CORPORATION·07613327071962·Smartgrip Pistol Battery Module

    IMMULITE PHENOBARBITAL, MODELS LKPB1, LKPB5

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    DISPOSABLE INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VYPRO MESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·November 9, 2010

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 26, 2012