BEUDAMED
    38 results · 21ms · Sources: EU EUDAMED, US FDA

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    STENTUBE LACRIMAL INTUBATION SET

    FDA 510(k)
    FDA Unclassified ·Unknown

    JOBST forMen Casual

    FDA UDI
    BSN MEDICAL, INC.·00035664131180·FOR MEN CASUAL 20-30 MM HG KNEE HIGH CLOSED TOE...

    n/a

    FDA UDI
    Ortho Development Corporation·00822409076505·Trial Head 28mm + 0

    General Instrument

    FDA UDI
    Life Spine, Inc.·00190837085148·

    Stablecut®

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00846795009886·

    Stablecut®

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024493797·

    MODIFICATION TO ALPHA DX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    REVLITE Q-SWITCHED ND: YAG LASER SYSTEM WITH NADPIECE ADAPTOR

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

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 15, 2021

    T:SLIM G4 SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OYC·November 30, 2017

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 14, 2024

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 11, 2021

    MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 32 SIZE S -4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·March 31, 2022

    CONTOUR NEXT

    FDA Adverse Event
    Injury ·ASCENSIA DIABETES CARE US INC·Product code NBW·March 5, 2018

    IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)

    FDA Adverse Event
    Malfunction ·Product code LLZ·February 28, 2014

    AIR DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·May 9, 2013

    11/13 S-ROM 44MM M SPEC+3

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code LPH·May 20, 2011

    UNK CODMAN SHUNT

    FDA Adverse Event
    Injury ·Product code JXG·October 14, 2016

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 10, 2015

    HANCOCK

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·December 20, 2019