BEUDAMED
    11 results · 26ms · 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 ×

    CrossFT Knotless Deep Thread Suture Anchor with Disposable Driver

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SOLSTICE

    FDA 510(k)
    FDA Class 2 ·Dental

    WIS1000

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

    MOBILELINK ACETABULAR CUP SYSTEM

    FDA Adverse Event
    Malfunction ·WALDEMAR LINK GMBH & CO. KG·Product code LPH·February 20, 2025

    I-STAT EC8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CHL·March 6, 2019

    LINER: CC E CC LIGHT FLAT PE HC LINER 32 / C

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·May 19, 2020

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 17, 2014

    6000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEIVE GROUP·Product code FRN·June 11, 2013

    GENTLEPOWER LUX CONTRA ANGLE 25LPA

    FDA Adverse Event
    Malfunction ·KAVO DENTAL GMBH·Product code EFB·July 4, 2011

    CUP: VERSAFITCUP CC TRIO Ø 48

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·May 2, 2019

    Smith&Nephew SmartStitch PerfectPasser Connector, REF # OM-8010, Rx Only, CE 0123, UDI: 00817470006971

    FDA Enforcement
    Class II ·Terminated·ArthroCare Corporation·September 30, 2020