BEUDAMED
    304 results · 28ms · 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 ×

    Powder Free Nitrile Examination Gloves Tested For Use With Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ProLift Trial

    FDA UDI
    Life Spine, Inc.·00190837087340·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100349·FEMTO SPECULUM FLAT WIRE

    Flextrode

    FDA UDI
    COSMAN MEDICAL, LLC·08132500133826·Electrode 15cm, 13mm Tip, 20G

    NA

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·00813250013382·Flextrode, 15cm,17G Introducer

    FASTPACK TSH IMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SFI-BAR (R) IMPLANT ADAPTER SPI (R) ELEMENT PF 0 4.0 / H 3.0 / H 4.0 / H 5.0 / H 6.0, SFI-BAR (R) IMPLANT ADAPTER STRA..

    FDA 510(k)
    FDA Class 2 ·Dental

    PULSAR MAX

    FDA Adverse Event
    Injury ·GUIDANT CLONMEL IRELAND·Product code NVZ·July 6, 2011

    KOTEX NATURAL BALANCE

    FDA Adverse Event
    Malfunction ·KIMBERLY-CLARK CORPORATION - CONWAY MILL·Product code HEB·June 7, 2013

    SETROX S 53

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·September 4, 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

    BD PHOENIX¿ NMIC/ID-307

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