BEUDAMED
    8 results · 19ms · 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.

    HP M2376A DEVICE LINK SYSTEM

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

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993587·anteriors; shade BL2; mould UIL

    DENTAL MERCURY

    FDA 510(k)
    FDA Class 2 ·Dental

    Sutter Swyng non-stick bipolar forceps, single-use

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

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    KENSTONE METAL·Product code ITJ·March 7, 2013

    CCU BED W/SCALE

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·January 24, 2011

    XENFORM

    FDA Adverse Event
    Other ·TEI BIOSCIENCES, INC.·Product code FTM·July 28, 2014

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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