BEUDAMED
    8 results · 20ms · 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.

    SUCTION CATHETER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PE Mouse IgG2a, K Isotype Ctrl

    FDA UDI
    BIOLEGEND, INC.·00810034700803·URL: https://www.biolegend.com/en-us/products/p...

    BracePaste MTP Light Cure Primer

    FDA 510(k)
    FDA Class 2 ·Dental

    NON-STERILE, POWDERED LATEX EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 28, 2013

    PROXIMATE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDW·January 27, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·August 5, 2014

    3.5MM TI LCP® PLATE 10 HOLES 137MM

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code KTT·August 4, 2025