BEUDAMED
    15 results · 25ms · 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 ×

    Disposable Blood Lancet (Soft Pro); Disposable Blood Lancet (Softsure); Disposable Blood Lancet (Softsure Pro); Disposable Blood Lancet (Softsense)

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

    BAREWIRE

    FDA UDI
    ABBOTT VASCULAR INC.·08717648137808·BareWire Workhorse Filter Delivery Wire 315 cm

    Medline UNITE Ancillary Foot Recon Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface

    FDA 510(k)
    FDA Class 2 ·Radiology

    2244031-1999-00003

    FDA Adverse Event
    Other ·December 30, 1999

    2244031-1999-00002

    FDA Adverse Event
    Other ·December 30, 1999

    2244031-1999-00001

    FDA Adverse Event
    Other ·December 30, 1999

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·January 12, 2018

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 11, 2014

    ACTIVA PC

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·August 24, 2011

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2013

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·October 22, 2018

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·March 12, 2019

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·December 20, 2017

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·December 20, 2017