BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    BRANAN MEDICAL CORPORATION MONITECT PCP DRUG SCREEN TEST, MODEL 160C AND 160D

    FDA 510(k)
    FDA Unclassified ·Unknown

    CliP Partial Prosthesis Titanium

    FDA UDI
    Heinz Kurz GmbH·EHKM10022721·Ossicular Prosthesis, partial

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092102671·Astra®-compatible Lilac 4.5/5.0mm Esthetic Abut...

    GRADIA®

    FDA UDI
    Gc America Inc.·14548161075299·GRADIA® DIRECT Unitips: 10 tips - 0.16 mL B1

    GRADIA®

    FDA UDI
    Gc America Inc.·D0470022721·GRADIA® DIRECT Unitips: 10 tips - 0.16 mL B1

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 29, 2021

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·November 5, 2020

    RSG-14-13, F/G #0002272

    FDA UDI
    RANFAC CORP.·00858690006273·RSG-14-13, F/G #0002272 PN 76010-01M

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QJR·April 14, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH,INC.·Product code QJR·April 14, 2021

    XIA SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HARDYDISK, NITROFURANTOIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PROCLAIM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 1, 2017

    SOLETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·June 14, 2012

    ARCHITECT IPTH

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code CEW·March 13, 2013

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011

    UNK DEPUY FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSA·February 20, 2008

    ORTHOPEDIC SALVAGE SYSTEM POLYETHYLENE TIBIAL BUSHING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018

    ORTHOPEDIC SALVAGE SYSTEM POLYETHYLENE FEMORAL BUSHING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018

    ORTHOPEDIC SALVAGE SYSTEM LOCKING PIN

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018