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

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    SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526743755·ACHIMED ACHILLES SUPP SAND VI

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526785052·EPICOMED ELB SUPPORT SAND VI

    NA

    FDA UDI
    Synthes GmbH·10886982141552·1.5MM CORTEX SCREW SELF-TAPPING 16MM

    Conventional Lead Apron .5mm Small 22 X 33

    FDA UDI
    Flow X Ray Corporation·00843696123031·Conventional Lead Apron .5mm Small, Medium Blue

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B523100035200816·PLIF CAGE, NON-LORDOTIC, 20AP X 08ML X 16HT

    IRON-PC-SL ASSAY MODEL # 151-10, 151-26

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SHARP BRAND ACUPUNCTURE NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·March 31, 2012

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·February 14, 2019

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·February 8, 2019

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·February 14, 2019

    TOTAL ASR ACET IMP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·October 24, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·August 8, 2011

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 2, 2013

    UNK RIGIDFIX CROSSPIN

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MAI·August 25, 2016

    BD MICROLANCE 3 NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMK·December 9, 2020

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·March 18, 2014

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HRS·March 18, 2014

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·March 18, 2014