BEUDAMED
    24 results · 23ms · 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 ×

    PANBIO INDX IGM DIP-S-TICKS LEPTOSPIROSIS TEST FOR THE DETECTION OF IGM ANTIBODIES TO LEPTOSPIRA BIFLEXA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Duesseldorf Type Bell Partial

    FDA UDI
    Heinz Kurz GmbH·EHKM10020241·Ossicular prosthesis, partial

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092002024·artVeneer life upper posteriors, M, A3

    LF

    FDA UDI
    Shenzhen Boon Medical Supply Co., Ltd.·06938327906252·90"(2300 mm) Y Tubing with Dual Check Valves(DE...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659162723·2.0 Cortex Screw, hex, St.Steel, L 24 mm_x000D_...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523132287·2-Level Anterior Cervical Plate, 24mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149568·12mm Insertion Guide

    PASS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLUROPERM 60-OK, PARAGON HDS-OK

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    RADOVAN TISSUE EXPANDER

    FDA Adverse Event
    MENTOR CORP.·Product code LCJ·May 17, 1994

    IPC® HANDPIECE - XPS® STRAIGHTSHOT® M4

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·November 15, 2015

    UNKNOWN SALINE IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·August 19, 2021

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·March 13, 2013

    PUMP/GRAVITY SOLUTION NO 'Y' SITE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code FPA·February 27, 2011

    ICY HOT HEAT THERAPY

    FDA Adverse Event
    Other ·CHATTEM, INC·Product code IMD·February 20, 2008

    MICRODEBRIDER 1898200T IGS M4

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·May 15, 2014

    UNK-CV-SR

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·May 13, 2024

    UNK-CV-SR

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·May 13, 2024

    BASE UNIT SERVO-U

    FDA Adverse Event
    Injury ·MAQUET CRITICAL CARE AB·Product code CBK·June 13, 2024

    BASE UNIT SERVO-U

    FDA Adverse Event
    Injury ·MAQUET CRITICAL CARE AB·Product code CBK·June 13, 2024