BEUDAMED
    37 results · 23ms · 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.

    ARKIT HBA1C

    FDA 510(k)
    FDA Class 2 ·Hematology

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496030553·VENERE 30, SIZE XXL, FUMO, GRADUATED COMPRESSIO...

    BUSCH®, BNA®

    FDA UDI
    BUSCH & CO. GmbH & Co. KG·D8120305531·Diamond, cone rounded edge, extra fine grit, ye...

    0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PRECISION XTRA BLOOD GLUCOSE TEST STRIP WITH TRUEMEASURE TECHNOLOGY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 8, 2026

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 8, 2026

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 8, 2026

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 8, 2026

    21GX.75IN. BD VACUTAINER® WINGED SAFETY PBBCS WITH 12 IN TUBING

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·November 27, 2017

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 21, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 18, 2026

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET PRE-ATTACHED HOLDER 23G NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 3, 2017

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 21, 2026

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 25, 2026

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·April 2, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 9, 2011

    ON-Q SILVERSOAKER

    FDA Adverse Event
    Other ·I-FLOW CORP.·Product code MEB·April 17, 2008