BEUDAMED
    104 results · 22ms · 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 ×

    FILTER CARESTAR 30; FILTER SAFESTAR 55; FILTER/HME TWINSTAR 55

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290114690324·Abutment Screw M1.6 Direct Conical

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108692358·Conical 2mm Straight Ball Abutment Ti

    ASI RPR Dropper Needle Cover

    FDA UDI
    ARLINGTON SCIENTIFIC, INC.·00816057021239·Blunt, 20 gauge needle cover

    SUREFIT DISPERSIVE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VIKING OPTIMA GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL)

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LKK·July 17, 2002

    4.0MM TI CORTEX EXPANSIONHEAD SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·September 4, 2002

    POLE MOUNT PRESS, MONIT. SYST.

    FDA Adverse Event
    Malfunction ·HEYER-SCHULTE NEUROCARE, INC.·Product code JXG·July 30, 2002

    AFFINITY

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code FNL·July 29, 2002

    TOTAL CARE

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code FNL·July 16, 2002

    SPECIALITE

    FDA Adverse Event
    Other ·HILL-ROM ARCHITECTURAL PRODUCTS HILL-ROM CO. INC.·Product code KZF·July 31, 2002

    OPTI FREE EXPRESS NO RUB DISINFECTION FORMULA

    FDA Adverse Event
    Other ·ALCON LABORATORIES, INC.·Product code LPN·July 12, 2002

    REMANUFACTURING BED

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code FNL·August 15, 2002

    AFFINITY

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code FNL·July 31, 2002

    ADVANTA BED

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code FNL·July 15, 2002

    PULMONETIC

    FDA Adverse Event
    Malfunction ·PULMONETIC SYSTEMS, INC.·Product code CBK·August 22, 2002

    ARROW

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code CAZ·August 15, 2002

    PULMONETIC

    FDA Adverse Event
    Malfunction ·PULMONETIC SYSTEMS, INC.·Product code CBK·August 6, 2002