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

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    SAMARCO SPIDER PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001271·artVeneer life upper anteriors, BOL, B4

    Silicone Tubing

    FDA UDI
    INVOTEC INTERNATIONAL, INC.·00818501023103·Silicone Tubing 0.250" X 0.438"

    Universal Dilator

    FDA UDI
    SPINEOLOGY INC.·M7401001271·Snap Lock Ring

    DELTA 16 TACT

    FDA 510(k)
    FDA Class 2 ·Radiology

    HARDYDISK, SULFA/TRIMETH

    FDA 510(k)
    FDA Class 2 ·Microbiology

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 9, 2016

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 9, 2016

    INTROCAN SAFETY

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·February 28, 2013

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·February 24, 2011

    THERMOPHORE AUTOMATIC MOIST HEAT PACK

    FDA Adverse Event
    Malfunction ·BATTLE CREEK EQUIPMENT COMPANY·Product code IRT·February 18, 2008

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·February 9, 2016

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    N2O SPHERICAL PROBE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HQA·June 9, 2021

    BIOLOX DELTA LNR 32MM 50-52MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·April 26, 2021

    UNKNOWN BIOLOX DELTA HEAD 32

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·April 26, 2021

    INTACS CORNEAL IMPLANTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    HAND PIECE FOR BATTERY POWERED DRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HWE·May 23, 2013