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

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    CONSENSUS CS2 PLUS ACETABULAR INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Premier

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·00856402006276·Decan Stopper Size 2 Closure Full

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964065095·Endo Carry-on Procedure Kit includes Suction Tu...

    "Ella" Protective Eyewear

    FDA UDI
    HAGER WORLDWIDE, INC.·D2481009330·Protective eyewear

    Copper Ni-Ti - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989027471·COPPER NITI 35 BAF 17X025UP LG PK10

    V.A.T.S. GEISSENDORFER DISSECTING FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896010550·V.A.T.S. GEISSENDORFER DISSECTING FORCEPS WITHO...

    V.A.T.S. GEISSENDORFER DISSECTING FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921009330·V.A.T.S. GEISSENDORFER DISSECTING FORCEPS WITHO...

    FERRIS SMITH UPPER KERRISON #1

    FDA UDI
    W.H. Holden, Inc.·D9281009330·

    AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SEAL-ON TOPICAL HEMPSTATIC POWDER SPRAY

    FDA 510(k)
    FDA Unclassified ·Unknown

    GYNECARE TVT-ABBREVO MINI LCM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·November 30, 2021

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 19, 2014

    XL FIXATION CAGE

    FDA Adverse Event
    Malfunction ·NUVASIVE SPINE·Product code KWQ·May 19, 2011

    ACT ARTIC E1 HIP BRG 28X38MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·February 18, 2016

    M2A 38MM MOD HD -3MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·February 18, 2016

    M2A-38 CUP NON FLARED SZ 52MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 21, 2016

    TAPERLOC POR LAT FMRL 9X137

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 21, 2016

    28MM MOD HD COCR -6MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·February 18, 2016

    DISPOSABLE STERILE HIGH TEMPERATURE ELECTROCAUTERY (HTC) F7244

    FDA Adverse Event
    Injury ·FIAB SPA·Product code GEI·October 12, 2023