BEUDAMED
    40 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 ×

    SPACELABS MEDICAL PATIENT MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    JOBST Bella Strong

    FDA UDI
    BSN MEDICAL, INC.·00035664010683·BELLA STRONG 30-40 MM HG ARMSLEEVE KNIT WELT SI...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383502306·Gutta Percha Points is used to root canal filin...

    BACT/ALERT FA PLUS (PLASTIC) ®

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·June 13, 2024

    VARPR 3.5MM 90 SUCTION ELECTRODE FOR USE WITH VAPR SYSTEM

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

    K-ASSAY D-DIMER CONTROLS

    FDA 510(k)
    FDA Class 2 ·Hematology

    BACT/ALERT FA PLUS (PLASTIC) ®

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·June 13, 2024

    BACT/ALERT FA PLUS (PLASTIC) ®

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·June 13, 2024

    BACT/ALERT FA PLUS (PLASTIC) ®

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·June 13, 2024

    BACT/ALERT FA PLUS (PLASTIC) ®

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·June 13, 2024

    BACT/ALERT FA PLUS (PLASTIC) ®

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·June 13, 2024

    BACT/ALERT FA PLUS (PLASTIC) ®

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·June 13, 2024

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·January 16, 2019

    ULTRAPRO HERNIA SYSTEM

    FDA Adverse Event
    Injury ·ETHICON, INC·Product code FTL·May 9, 2013

    PERCUTANEOUS THROMBOLYTIC DEVICE KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNACIONAL INC.·Product code MCW·August 27, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 20, 2011

    PERITX DRAINAGE BAG

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code PNG·April 3, 2026

    PERITX DRAINAGE BAG KIT

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code PNG·December 18, 2025

    PERITX DRAINAGE BAG

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code PNG·April 11, 2026

    PERCEPT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·December 16, 2020