BEUDAMED
    9 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.

    STERILE HYDROGEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993119·anteriors; shade A3.5; mould UCM

    Bipolar forceps

    FDA UDI
    SOPRO-COMEG GmbH·04059082014814·

    Twin-Pass Dual Access Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARGENCO 1

    FDA 510(k)
    FDA Class 2 ·Dental

    V-18¿ CONTROL WIRE¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code DQX·March 7, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 16, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026