BEUDAMED
    69 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 ×

    INBONE II TOTAL ANKLE REPLACEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964061400·Endo Carry-on Procedure Kit includes Biohazard ...

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964070761·Endo Carry-On Procedure Kit

    NITANIUM® ARCHWIRES

    FDA UDI
    Ortho Organizers, Inc.·00190707065706·.016 X .022 Upper Coated Nitanium® Pro Form™ Ar...

    Monoblock Tibial Trial UC Insert

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215043681·

    MAXCUT DIAMOND BURS (6/pk) MED 886-014

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D778100886141·MAXCUT DIAMOND BURS (6/pk) Shape: Pointed Cylin...

    MAXCUT DIAMOND BURS (6/pk) MED 886-016

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D778100886161·MAXCUT DIAMOND BURS (6/pk) Shape: Pointed Cylin...

    SPIROL EPIDURAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SIMPLICITY WING INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·May 24, 2011

    ENDO GIA UNIVERSAL 12MM SINGLE USE INST

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·August 6, 2008

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code OKS·August 19, 2014

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 13, 2017

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 5, 2017