BEUDAMED
    190 results · 26ms · 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 ×

    HBA1C CONTROL, LEVEL 1 AND LEVEL 2

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10887488334288·CUSTOM TRAY

    PARALLEL BAR,FLDNG,HT ADJ,SPEC CONST 2PC

    FDA UDI
    Hausmann Enterprises, LLC·00840314800091·

    MetaSystems Probes

    FDA UDI
    MetaSystems Probes GmbH·04251315801097·XL t(4;11) AFF1/KMT2A DF, 10x 100µl,Translocati...

    KAIYANG STEEL WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ELEKTA LEKSELL STEREOTACTIC SYSTEM WITH MR POST KIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·February 10, 2000

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·December 15, 1999

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Death ·DATASCOPE CORPORATION·Product code DSP·April 7, 1999

    DISTAFLO BYPASS GRAFT

    FDA Adverse Event
    Injury ·IMPRA, A SUBSIDIARY OF C. R. BARD, INC.·Product code DSY·January 28, 2000

    UNK

    FDA Adverse Event
    Other ·SAFESKIN CORP.·Product code LYY·January 13, 2000

    OLYMPUS

    FDA Adverse Event
    Malfunction ·OLYMPUS OPTICAL CO., LTD·Product code GCT·August 20, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    ASSURANCE 2000 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·September 13, 1999

    SMOOTH SALINE MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FWM·June 4, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·February 5, 1999

    ENDOPATH CLAW EXTRACTOR

    FDA Adverse Event
    Malfunction ·SYMBIOSIS CORP.·Product code KNS·February 16, 1998

    8F ANGIO-SEAL HEMOSTATIC PUNCTURE CLOSURE DEVICE

    FDA Adverse Event
    Injury ·DAIG CORP.·Product code MGB·November 16, 1999

    UNK

    FDA Adverse Event
    Other ·SAFESKIN CORP.·Product code LYY·April 8, 1999