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 ×

    JASUN, MODELS DT-01F AND DT-11F

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MAC

    FDA UDI
    Ge Medical Systems Information Technologies, Inc.·00198953107263·MAC VU360 V3.00 SW UPGRADE

    Statcorp Medical

    FDA UDI
    Statcorp Medical·10841522119118·HOSE,AIR,6FT,FEMALE BAYONET FITTINGS,EA

    RENEW LS-2

    FDA 510(k)
    FDA Class 2 ·Dental

    K-ASSAY AT-III

    FDA 510(k)
    FDA Class 2 ·Hematology

    XIA LP POLYAXIAL SCREW 6.5 X 40MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·September 20, 2011

    XIA ROD DIA. 6 X 480

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·June 2, 2011

    XIA BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·May 2, 2011

    XIA SCREW 6, 5 X 40

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code MNI·May 11, 2011

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·November 2, 2022

    XIA LP POLYAXIAL SCREW 5.5 X 45MM

    FDA Adverse Event
    Injury ·STRYKER SPINE-SWITZERLAND·Product code KWP·September 7, 2016

    XIA POLYAXIAL SCREW 8.5 X 40MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code MNH·May 2, 2011

    XIA BLOCKER

    FDA Adverse Event
    Injury ·STRYKER SPINE BORDEAUX·Product code KWP·May 11, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 2, 2013

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·March 7, 2011

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·April 16, 2008

    ASPHERE M SPEC 12/14 40 +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 23, 2012

    PINNACLE MTL INS NEUT40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 23, 2012

    XIA LP POLYAXIAL SCREW 6.5 X 50MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·September 20, 2011

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·March 8, 2023