BEUDAMED
    12 results · 33ms · 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 ×

    A-DEC PERFORMER CONTROL UNIT

    FDA 510(k)
    FDA Class 1 ·Dental

    Nexxis OR

    FDA UDI
    Barco NV·05415334033047·NEXXIS SYSTEM X620 CM V3

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295232940·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING TC3 1....

    Eye Shield

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111178·EYE SHIELD CLEAR PLASTIC PACK OF 12

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930796050610·Suction Tube 6FR 120mm 45 degree

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930796050620·Nasal Suction Tube Angled 30 Deg 6FR

    MICROSPAN SYSTEM

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code FED·June 8, 2006

    Planmeca ProMax 3D Max, Planmeca Maximity

    FDA 510(k)
    FDA Class 2 ·Radiology

    STRYKER SPINE VLIFT VERTEBRAL BODY REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    2520274-2013-10231

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 11, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 13, 2011

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·July 15, 2014