BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    Non-sterile, Powder-Free Nitrile Examination Glove Black Tested for use with Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Halyard

    FDA UDI
    Avanos Medical, Inc.·10680651934359·PMP,EP TRY,S-SHOT,-,-,10

    Ceramco® II Silver™

    FDA UDI
    Dentsply International Inc.·D0011822410·

    TIBIAL NAIL, STANDARD 10X390 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·March 17, 2010

    THE DALE ACE CONNECTOR (ACCESS CONTROLLER FOR ENTERAL), MODEL H84104751

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

    ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT

    FDA 510(k)
    FDA Class 1 ·Dental

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. CRMD·Product code NVN·January 13, 2014

    STEALTHSTATION TREON TREATMENT GUIDANCE SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·July 12, 2011

    SOFTCLIX ® LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·June 21, 2013

    Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airway connector.

    FDA Enforcement
    Class II ·Terminated·Intersurgical Inc·January 15, 2020

    URETERAL BRUSH BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FDX·November 15, 2023

    URETERAL BRUSH BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FDX·January 7, 2022