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

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    L720 EXAMINATION CHAIR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092122693·Straumann Tissue Level RN x 4.5mm Titanium Base

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040044261·Forcep Extracting

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001261·artVeneer life lower anteriors, UIL, B3

    Silicone Tubing

    FDA UDI
    INVOTEC INTERNATIONAL, INC.·00818501023097·Silicone Tubing 0.250" X 0.375"

    ULTRAPEN REUSABLE PENCIL, MODEL 130350 THROUGH 130353, REUSABLE ACCESSORY ELECTRODE KIT (FOR USE WITH ULTRAPEN PENCIL),

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

    HARDYDISK, PIPERACILLIN/TAZOBACTAM, 110MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·November 26, 1997

    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

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·February 26, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 25, 2011

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC·Product code JAA·February 22, 2008

    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·February 9, 2016

    INTACS PRESCRIPTION INSERTS

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

    WA4000 20# N20 CONN

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·May 28, 2020

    CORTICAL BONE SCREW, ÿ 4X28MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·March 4, 2022

    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