BEUDAMED
    11 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 ×

    EMPRINT ABLATION SYSTEM

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

    Oticon

    FDA UDI
    Oticon A/S·05707131264732·RIA PRO, KIT 13 WL DIR 90 R H BE

    Hermann Medizintechnik GmbH

    FDA UDI
    Hermann Medizintechnik GmbH·04059453024961·Insert, Alligator forceps, Ø10mm,WL 330mm, doub...

    K133801

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 31, 2024

    TRANSONIC COSTATUS CARDIAC OUTPUT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 26, 2021

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 27, 2020

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 1, 2014

    BIPOL LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·May 29, 2013

    CONVECTIVE PATIENT WARMER

    FDA Adverse Event
    Malfunction ·STRYKER CORP DBA GAYMAR·Product code DWJ·May 12, 2011