BEUDAMED
    18 results · 18ms · 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.

    COLOR CODED PUTTY SOFT, REGULAR & FIRM

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950022403·CALIPER CASTROVIEJO SHORT BEAK STRAIGHT 0-40MM ...

    WorkMate Claris™

    FDA UDI
    ST. JUDE MEDICAL, INC.·05415067047175·Z440 Software Upgrade Kit

    HEARTLINE MINI JAW NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896011359·HEARTLINE MINI JAW NEEDLE HOLDER WITH LOCK TUNG...

    HEARTLINE MINI JAW NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09928000170·HEARTLINE MINI JAW NEEDLE HOLDER WITH LOCK TUNG...

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989051216·UPPER LEFT FIRST MOLAR TRIMLINE BAND SIZE 17

    Rampart O

    FDA UDI
    SPINEOLOGY INC.·M7402800017·13x30mm Trial

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHOYCE MARK VIII ANTERIOR CHAMBER INTEROCULAR LENS

    PARSET SECONDARY ADMINISTRATION SET, LUERLOCK, MODEL A14001E, PARSET SECONDARY SECONDARY ADMINISTRATION SET, MODEL A1400

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VIDAS AFP ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHOYCE MARK VIII ANTERIOR CHAMBER INTEROCULAR LENS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHOYCE MARK VIII ANTERIOR CHAMBER INTEROCULAR LENS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHOYCE MARK VIII ANTERIOR CHAMBER INTEROCULAR LENS

    STAT DL 9.5 34 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·January 15, 1998

    RESTORE ADVANCED

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 8, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 17, 2012

    SYNERGY

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·August 12, 2010

    Model: CT 5300; Product Code (REF): 728285; Software Versions: 5.1.0.X & 5.1.1.X;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS·November 5, 2025