BEUDAMED
    617 results · 31ms · Sources: EU EUDAMED, US FDA

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    STRYKER DISPOSABLE CRANIAL PERFORATOR BIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694038836·2.0mm x 10mm Midface Screw

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193101989·EVOS Rotate HA PEEK 10mm x 9mm x 26mm Flat, 8°

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR76000820101·Lingual cleat on pad max. left / mand. right

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0120100·Assembly, Screwdriver, NIDO Assembled Screws

    STC METHADONE INTERCEPT MICRO-PLATE EIA, MODEL 11421

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MODIFICATION TO LR 5200 FILM RECORDER

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH. LTD. / HUNTINGTON·Product code MFK·March 19, 2010

    WHATMAN BODY FLUID COLLECTION PAPER '903'

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE, BIO-SCIENCES CORP.·Product code JKA·March 10, 2011

    OPTI-FREE REPLENISH

    FDA Adverse Event
    Injury ·ALCON - FORT WORTH / ALCON LABORATORIES, INC.·Product code LPN·January 7, 2011

    AMS INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·October 31, 2013

    ISPAN SULFUR HEXAFLUORIDE (SF6) GAS

    FDA Adverse Event
    Injury ·ALCON - FORT WORTH/ALCON LABORATORIES, INC.·Product code LPO·February 4, 2010

    MIDMARK

    FDA Adverse Event
    Malfunction ·MIDMARK CORP.·Product code GBB·April 18, 2011

    THERAPY ABLATION CATHETER

    FDA Adverse Event
    Malfunction ·IRVINE BIOMEDICAL, A ST. JUDE MEDICAL COMPANY·Product code OAD·September 29, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·March 17, 2010

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·May 3, 2010

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·August 6, 2010

    TYVASO INHALATION SYSTEM

    FDA Adverse Event
    Malfunction ·UT GMBH·Product code CAF·September 6, 2012

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 29, 2013

    COMBO CATH WIRE-GUIDED CYTOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FDX·May 9, 2011