BEUDAMED
    11 results · 35ms · 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 ×

    WATERS 717 AUTOSAMPLER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Sonoma

    FDA UDI
    Seaspine Orthopedics Corporation·10889981086848·Castroviejo Caliper

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122932·K-WIRE - DOUBLE TROCAR 1.25mm DIA x 150mm

    EMBRYOGEN

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    VISUALINE BARBITURATES DIPSTRIP TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SECONDARY IV SET-SL/CE (50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·March 12, 2012

    AVAULTA SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code FTL·December 8, 2010

    3002 MASTER BOMS

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 17, 2013

    HEARTWARE VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·July 8, 2014

    LAPIPLASTY SYSTEM S4A

    FDA Adverse Event
    Injury ·TREACE MEDICAL CONCEPTS, INC.·Product code HRS·March 14, 2025

    LIGACLIP

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·September 26, 2017