BEUDAMED
    352 results · 20ms · 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 ×

    MEDCOMP T-3

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

    Baltic Denture System BDLoad

    FDA UDI
    Merz Dental GmbH·D7091033570·Baltic Denture System BDLoad BDLoad Mm7 PLSEbi...

    DIRECTVIEW CR Long-Length Cassette with PQ Screen

    FDA UDI
    CARESTREAM HEALTH, INC.·60889971033574·CR LLI W/PQ SCREEN

    Gibralt®

    FDA UDI
    INNO Holdings, Inc.·M711050020335700·Posterior Cervical, Rod, Prebent, Ti, 3.5mm x 7...

    Gibralt

    FDA UDI
    Choice Spine, LP·10885862223135·

    OSSEOTITE DENTAL IMPLANTS

    FDA 510(k)
    FDA Class 2 ·Dental

    BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TI-DBLE LEAD CORT SCR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSB·August 24, 2018

    QC F/K-WIRES Ø0.6-3.2 F/COMPACT AIR DRIV

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·April 3, 2013

    RESOLVE PANEL B

    FDA Adverse Event
    Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code KSZ·March 30, 2011

    DXTEND MBLOC HUM EPI 1 D12 STD

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A.·Product code HSD·April 23, 2008

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 20, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025