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

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    CARESIDE HEMOGLOBIN

    FDA 510(k)
    FDA Class 2 ·Hematology

    Preat

    FDA UDI
    Preat Corporation·00842092170779·Straumann® BL RC-compatible Engaging Ti Base X ...

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964013247·The ENDO CARRY-ON Procedure Kit contains all of...

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65890014620·20/20 Light Curing Hybrid Composite (3G B3)

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092103876·Straumann Bone Level RC x 6mm Titanium Base

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001462·artVeneer life upper anteriors, CL, D3

    GOLDFINGER DEVICE

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

    URINE PHENCYCLIDINE (PCP) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF 94A

    FDA 510(k)
    FDA Unclassified ·Unknown

    RENALIN

    FDA Adverse Event
    Other ·MINNTECH CORP.·Product code LIF·April 4, 1994

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·April 16, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·January 27, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·February 24, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·November 6, 2025

    NEURON MAX 6F 088 LONG SHEATH

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·February 10, 2016

    NEURON MAX 6F 088 LONG SHEATH

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·February 10, 2016

    EXODONTIA ELEVATOR #46R SERRATED

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 29, 2016

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·March 5, 2013

    HEARTMATE II SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·January 26, 2011

    EAGLE EYE CATHETER

    FDA Adverse Event
    Other ·VOLCANO CORPORATION·Product code DQO·February 20, 2008

    EXODONTIA ELEVATOR #46R SERRATED

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 29, 2016