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

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    ALMA DIODE TABLETOP LASER

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

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075022170·CLOSED COIL SPRING STAINLESS 0.010 X 0.030 40IN...

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989043983·CROWN-PERM LL 5 1ST BICUSPID SST PK/5

    Merit® Kit

    FDA UDI
    Merit Medical Systems, Inc.·00884450256343·

    Merit® Kit

    FDA UDI
    Merit Medical Systems, Inc.·00884450137437·

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR21021400051·Compound retraction arch mand. .016"x.022" / 30°

    ZEUS-O

    FDA UDI
    SPINAL ELEMENTS·00840606151368·ZEUS®-O 5MM DILATOR

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·GENVISC 850

    PROFILE 2000/3000 LASER SYSTEM

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

    BD PEN NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·GenVisc 850

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·GenVisc 850

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·GenVisc® 850

    AMISTEM H HA COATED STD STEM SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·March 8, 2023

    AMISTEM H, HA COATED STEM SIZE 2 STD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·September 30, 2016

    BD INSULIN PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2015

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 3, 2014

    TRILOGY 202

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·May 28, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·June 25, 2011

    UNIVERSA LOOP NEPHROSTOMY PERCUTANEOUS DRAINAGE CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KOB·May 2, 2018