BEUDAMED
    31 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.

    H.M.T. ACUPUNCTURE NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    n/a

    FDA UDI
    Ortho Development Corporation·00822409072521·Blunt Tip Broach Size 1

    ICU Medical

    FDA UDI
    ICU MEDICAL, INC.·00840619023348·ChemoClave™ Vented Vial Spike

    Minute Stain - L.M.D. Elixirs

    FDA UDI
    Taub Products·D8370125010·Minute Stain's Larry’s Magical Denture Elixirs ...

    JOBST Custom Seamless Soft

    FDA UDI
    BSN-Jobst GmbH·04059993137336·CUSTOM SEAMLESS SOFT 3/AG-HT ONE LEG PANTY/CLOS...

    JOBST Custom Seamless Soft

    FDA UDI
    BSN-Jobst GmbH·04059993131815·CUSTOM SEAMLESS SOFT 1/AG-HT ONE LEG PANTY/CLOS...

    JOBST Custom Seamless Soft

    FDA UDI
    BSN-Jobst GmbH·04059993139521·CUSTOM SEAMLESS SOFT 2/AG-HT ONE LEG PANTY/CLOS...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694012294·Single Silicone Tubing Set, 12 ft. (Clips Inclu...

    Phonak

    FDA UDI
    Phonak AG·07613275044933·Phonak Dalia 13 UZ Petite

    SMARTSCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENDOPOUCH RETRIEVER

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

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180503683·Tip, Curette, Cup, Size 2, Straight, Smooth

    K1025-01-EDT

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·6 devices

    VIDAS Clostridium Difficile GDH, REF 30125-01

    FDA Recall
    Open, Classified ·bioMerieux, Inc.·Product code MCB·September 22, 2021

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·March 20, 2013

    S4S/SUR-FIT NATURA 2 PC - 2 PC DURAHESIVE (DH)

    FDA Adverse Event
    Injury ·CONVATEC INC.·Product code EXE·August 12, 2014

    HIGH PRESSURE TUBING IN A CUSTOM KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code BYX·March 12, 2008

    VIDAS Clostridium Difficile GDH, REF 30125-01

    FDA Enforcement
    Class II ·Ongoing·bioMerieux, Inc.·January 5, 2022

    PREMICRON GREEN 4/0(1,5)4X45 HR13 TOM

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAT·January 29, 2020

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 9, 2022