BEUDAMED
    3,049 results · 26ms · 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 ×

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749036534·Mercedes thoracic retractor

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749036503·Blades for Mercedes retractor 50 x 65 mm fenest...

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749036510·Blades for Mercedes retractor 75 x 75 mm fenest...

    IMED PC-1

    FDA Adverse Event
    Injury ·ALARIS MEDICAL SYSTEM·Product code FRN·May 13, 2002

    UNSPECIFIED BD INFUSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·May 24, 2024

    HLM TUBING SET W/BIOLINE COATING

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·February 5, 2016

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 22, 2026

    REALITY CONDOMS

    FDA Adverse Event
    Injury ·THE FEMALE HEALTH CO.·Product code MBU·June 23, 2021

    FC1 FEMALE CONDOM

    FDA Adverse Event
    Injury ·THE FEMALE HEALTH CO.·Product code MBU·June 25, 2009

    REALITY

    FDA Adverse Event
    Malfunction ·FEMALE HEALTH CO.·Product code MBU·June 25, 1997

    8044101-2001-00001

    FDA Adverse Event
    Other ·Product code MBU·June 5, 2001

    FC FEMALE CONDOM

    FDA Adverse Event
    Other ·THE FEMALE HEALTH CO.·Product code MBU·June 5, 2001

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·September 3, 2025

    BARDEX® LUBRI-SIL® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZL·August 27, 2025

    UNKNOWN LATEX FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·August 22, 2025

    BD PYXIS¿ ES SERVER

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·September 16, 2025

    Single-Use Internal Condom

    FDA classification
    FDA Class 2 ·Single-Use Internal Condom

    AMBU SDN.BHD.

    FDA registration
    AMBU SDN.BHD.·14 products·🇲🇾 Malaysia

    AMBU Limited

    FDA registration
    AMBU Limited·11 products·🇨🇳 China

    Ambu A/S

    FDA registration
    Ambu A/S·27 products·🇩🇰 Denmark