BEUDAMED
    8 results · 18ms · 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.

    TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGY

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

    OPTICAL FRAME A285, A210, B220, A215, A255, B220,

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    E1 RINGLOC BIPOLAR 28X51MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·June 17, 2019

    BIOMEX SHELL PC DIA48MM LN 22

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 2, 2015

    ARIS TRANS OBTURATOR KIT

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FTL·January 22, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 10, 2014