BEUDAMED
    69 results · 23ms · Sources: EU EUDAMED, US FDA

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    LenSx Laser System

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169600195·TRIAL 2173660 O25 IB 20MM 18 DEG 18X60

    FlexBoard™ BTM-LX module

    FDA UDI
    MACROMEDICS B.V.·08720168161710·Breast Treatment Module LX for FlexBoard RealEase

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613055714·Bainbridge Thyroid Forceps, Straight, Overall L...

    38 MM MODULAR HEAD PROVISIONAL

    FDA UDI
    Biomet Orthopedics, LLC·00880304003101·

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111118647·BAINBRIDGE FCP STR 6"

    COLD PACK, PLASTIC APPLICATOR (MEDICAL GRADE)-NON-CHEMICAL

    FDA 510(k)
    FDA Unclassified ·Unknown

    LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CART 9733856 S7 STAFF ASSEMBLED 110V

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 18, 2019

    BIOMET

    FDA Adverse Event
    Injury ·BIOMET·Product code KWA·February 28, 2014

    M2A 38MMX54MM CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·April 28, 2023

    COMMUNICATOR

    FDA Adverse Event
    Malfunction ·EXTERNAL MANUFACTURER·Product code LWS·July 23, 2011

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 17, 2013

    ZM-930PA

    FDA Adverse Event
    Injury ·NIHON KOHDEN CORPORATION·Product code MHX·September 10, 2014

    MLRY-HD POR FMRL 9X150MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 25, 2019

    UNKNOWN ACTIVE ARTICULATION FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 15, 2018

    M2A-38 CUP NON FLARED SZ 54MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·July 5, 2018

    UNKNOWN MAGNUM SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·June 25, 2018

    M2A 38MM MOD HD -6MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 29, 2014

    CART 9733856 S7 STAFF ASSEMBLED 110V

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 6, 2019