BEUDAMED
    71 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Wingman 35 Crossing Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    38 MM MODULAR HEAD PROVISIONAL

    FDA UDI
    Biomet Orthopedics, LLC·00880304003132·

    RUBBERCARE POWDER FREE NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LZI METHAMPHETAMINE ENZYME MMUNOASSAY, LZI METHAMPHETAMINE CALIBRATORS, LZI METHAMPHETAMINE CONTROLS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    TAPERLOC MICROP FMRL 5.0MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·November 30, 2018

    M2A 38MM MOD HD -3MM NK

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

    M2A MAGNUM ACETABULAR SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 24, 2018

    ROTATABLE SNARE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code FDI·October 15, 2014

    M2A-MAGNUM PF CUP 54ODX48ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 17, 2013

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 23, 2011

    M2A-38 CUP NON FLARED SZ 56MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 19, 2018

    M2A FLARED ONE PIECE CUP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 30, 2017

    TAPERLOC POR LAT FMRL 17.5X155

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·October 1, 2019

    BALANCE MICROP STEM 12X80MM RT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·December 27, 2017

    BIOMET METAL-ON-METAL HIP SYSTEMS- EXPANDED CONTRAINDICATIONS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·April 7, 2017

    M2A-38 CUP NON FLARED SZ 56MM

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

    MODULAR POROUS LATERALIZED REDUCED DISTAL TAPERLOC FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 8, 2018

    TAPERLOC POR FMRL 13.5X147

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

    M2A-MAGNUM PF CUP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 8, 2017

    M2A 38MM MOD HEAD COMPONENT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 20, 2017