BEUDAMED
    24 results · 21ms · 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 ×

    BIOCHECK, INC. B-2 MICROGLOBIN ENZYME IMMUNOASAY TEST KIT, MODEL BC-1061

    FDA 510(k)
    FDA Class 2 ·Immunology

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001022·artVeneer life lower anteriors, UCS, A1

    QUASAR

    FDA UDI
    Modus Medical Devices Inc·G34310010220·MRI 4D Motion Phantom

    Monza Cervical Plate System

    FDA UDI
    Altus Spine, LLC·00843210121864·SSP: Screw Driver

    XCM Biologic® Tissue Matrix

    FDA UDI
    DSM BIOMEDICAL, INC.·00812337020220·

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989014129·EDGEWISE DOUBLE WIDTH BRKT 022

    QUASAR

    FDA UDI
    Modus Medical Devices Inc·G34310010222000·MRI 4D Motion Phantom - ViewRay Service Configu...

    Diamond Orthopedic, LLC

    FDA UDI
    DIAMOND ORTHOPEDIC, LLC·B551DMD2001022·2.4mm, Cannulated Screw, Self Drilling, Long T...

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF20010220·2.4mm Cannulated Screw, Self Drilling, Long Thr...

    CAPSTONE CONTROL SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·January 20, 2016

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540245809·POINTER, RIGHT POSTERIOR-FOSSA

    KineMatch® PFR System

    FDA UDI
    Kinamed, Inc.·00818720013114·Autoclave Case, Base

    COLLAGRAFT STRIP BONE GRAFT MATRIX (FOR USE AS A BONE FILLER), MODEL 1X,3X,6X (1,3 OR 6 STRIPS PER BOX)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HARDYDISK CEFAMANDOLE, 30MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Vermed

    FDA UDI
    GRAPHIC CONTROLS ACQUISITION CORP·00009336000210·Electrocardiographic recording paper

    FLOW-I C20 ANESTHESIA SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code BSZ·July 1, 2025

    XCM BIOLOGIC TISSUE MATRIX

    FDA Adverse Event
    Malfunction ·KENSEY NASH CORP.·Product code FTM·November 16, 2012

    IMPAX CV REPORTING

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

    UNKNOWN ZIMMER MIS TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·February 21, 2011

    ACCU-CHEK ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·February 20, 2008