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

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    Medifine Pen Needle 3 Bevel, Medifine Pen Needle Quinta 5 Bevel

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Oticon

    FDA UDI
    Oticon A/S·05707131319180·OPN 1, BTE 13 PP 2.4G 105 C063

    CANDELA GENTLELASE FAMILY OF LASERS

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

    MODIFICATION TO:RADIUS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 11, 2019

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·April 1, 2019

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 14, 2013

    ACCESS 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·July 1, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM

    FDA Adverse Event
    Injury ·BIOENTERICS CORP.·Product code LTI·September 18, 2008

    INTIMA-II Y 22GAX1.00IN PRN/EC SLM

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·January 13, 2021

    BD INTIMA-II CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·June 15, 2020

    OT ULTRALINK METER

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