BEUDAMED
    142 results · 23ms · 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 ×

    Ultrasound Transmission Gels

    FDA 510(k)
    FDA Class 2 ·Radiology

    Oticon

    FDA UDI
    Oticon A/S·05714464007585·EARQ F50 MINIRITE R C090

    GENERAL PURPOSE TEMPERATURE PROBE, SKIN TEMPERATURE PROBE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GRIPPER PLUS NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTEGRA ARTIFICIAL SKIN

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCE CORP.·Product code MDD·September 21, 1999

    INTEGRA ARTIFICIAL SKIN

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORP.·Product code MDD·September 21, 1999

    INTEGRA ARTIFICIAL SKIN

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORP.·Product code MDD·September 21, 1999

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·April 19, 1999

    ERA SHEATH

    FDA Adverse Event
    Injury ·CONCEPTUS, INC.·Product code FJL·October 14, 1998

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·April 9, 1999

    VASOSEAL VHD

    FDA Adverse Event
    Injury ·DATASCOPE CORP./COLLAGEN PRODUCTS·Product code MGB·April 26, 1999

    CAPIO SUTURE CAPTURING DEVICE

    FDA Adverse Event
    Malfunction ·MICROVASIVE UROLOGY A DIV. OF BOSTON SCIENTIFIC CORP.·Product code GCJ·November 16, 1999

    VESICA SLING KIT WITH PROTEGEN

    FDA Adverse Event
    Injury ·MICROVASIVE UROLOGY, BOSTON SCIENTIFIC CORP.·Product code FTL·April 21, 1999

    VERSYS HIP SYSTEM FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LZO·October 31, 2005

    INFUSE-A-CATH CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Other ·HORIZON MEDICAL PRODUCTS, INC.·Product code DQO·November 18, 1999

    UNK

    FDA Adverse Event
    Other ·SAFESKIN CORPORATION·Product code LYY·November 19, 1999

    273599

    FDA Adverse Event
    Injury ·November 10, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·August 11, 1999

    UNK

    FDA Adverse Event
    Other ·SAFESKIN CORPORATION·Product code LYY·July 19, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·July 22, 1999