BEUDAMED
    11 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 ×

    DePuy Synthes Static Staples

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197082877·CONVERSE, TC Needle Holder 120mm,...

    UNASSIGNED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IMPIX LUMBAR INTERBODY DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MPACT FLAT PE HC LINER Ø36/G

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·December 11, 2018

    MPACT FLAT PE HC LINER Ø36/F

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·November 9, 2018

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·July 27, 2011

    LIBERTÉ?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·June 20, 2013

    DUOVISC

    FDA Adverse Event
    Injury ·ALCON-BELGIUM/ S.A. ALCON-COUVREUR N.V.·Product code LZP·September 26, 2008

    SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS

    FDA Adverse Event
    Injury ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019

    CUP: MPACT ACETABULAR SHELL Ø52 TWO-HOLES

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·April 18, 2019