BEUDAMED
    86 results · 22ms · Sources: EU EUDAMED, US FDA

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    CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SideStream

    FDA UDI
    RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD·00383730001340·SideStream Plus (EU) with Filter, 10 pack.

    MODIFICATION TO FLEXVIEW CLINICAL MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRIPPER PLUS NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MJ7 "VISION" TEST DEVICE

    FDA Adverse Event
    Other ·MEDI-JECT CORP.·Product code KZE·October 5, 1999

    INTEGRA ARTIFICIAL SKIN

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORP.·Product code MGR·August 6, 1999

    ETHICON INC., JOHNSON & JOHNSON

    FDA Adverse Event
    Injury ·*·Product code GAM·March 23, 2000

    SOFTFORM FACIAL IMPLANT

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

    9550 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·August 6, 1999

    SOFTFORM FACIAL IMPLANT

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

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC INC·Product code DTB·October 14, 2002

    LP6+ VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·October 4, 1999

    SOFTFORM FACIAL IMPLANT

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

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·August 6, 1999

    SYNTHES

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code HTW·January 19, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·October 8, 1999

    LP6+ VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·April 27, 1999

    LP6+ VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·August 6, 1999

    PREMICATH

    FDA Adverse Event
    Death ·VYGON GMBH & CO KG·Product code DQO·February 29, 2000

    CIRCLE C SILICONE CATHETER KIT

    FDA Adverse Event
    Other ·HORIZON MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code LFJ·September 28, 1999