BEUDAMED
    10,000 results · 58ms · 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 ×

    dental diamond bur

    FDA UDI
    STRAUSS & CO - INDUSTRIAL DIAMONDS LTD·D87742179COMSET1KNT1·Dental Diamond Bur KIT

    Pinn Lite

    FDA UDI
    Harmar Summit, LLC·00817650026133·SL300 With Chassis Obstruction Sensors No Track

    Rave

    FDA UDI
    Harmar Summit, LLC·00817650024498·Rave-II Kit No Track

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780456865·Integra® Jarit® Knurled Nut for Ref# 205-310 (F...

    Rave

    FDA UDI
    Harmar Summit, LLC·00817650024436·Rave-II - LH Folding Rail Without Track

    Rave

    FDA UDI
    Harmar Summit, LLC·00817650024443·Rave-II - RH Folding Rail Without Track

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Injury ·COOK INC·Product code KNT·November 30, 2018

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Injury ·COOK INC·Product code KNT·December 3, 2018

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Injury ·COOK INC·Product code KNT·December 3, 2018

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNT·February 15, 2018

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNT·July 1, 2017

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNT·March 5, 2018

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNT·May 4, 2018

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Injury ·COOK INC·Product code KNT·April 27, 2016

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNT·June 29, 2017

    KNT TUBES, GASTROINTESTINAL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNT·July 12, 2019

    RECTAL INSERT

    FDA Adverse Event
    Injury ·WELLSPECT HEALTHCARE·Product code KNT·March 11, 2026

    TRI-FUNNEL REPL GAST 20F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code KNT·October 10, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code FGE·August 1, 2017

    TRI-FUNNEL REPL GAST 20F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code KNT·October 11, 2019