BEUDAMED
    351 results · 21ms · Sources: EU EUDAMED, US FDA

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    ASPIRE RX-LP6 ASPIRATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KAIYANG ALUMINUM WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    MODEL J-5 MVO-MONITOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC·Product code FTL·June 18, 1999

    INTRA-AORTIC BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·March 23, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·December 29, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·June 18, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·December 29, 1998

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO.·Product code MGB·April 16, 1998

    IOLAB

    FDA Adverse Event
    Injury ·CHIRON VISION·Product code HQL·June 26, 1998

    ZYDERM 1 COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·COLLAGEN CORP·Product code LMH·September 3, 1998

    STAT DL 9.5 FR. 34 CC. IAB, INTERNATIONAL

    FDA Adverse Event
    Death ·DATASCOPE CORP.·Product code DSP·October 16, 1998

    USSC MONOSOF 10/0

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAR·April 14, 1997

    USSC MONOSOF 10/0

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAR·April 14, 1997

    SUSTAIN 3.4X13 HA EXTERNAL HEX IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·November 11, 1998

    SUSTAIN 4X10 SCREW IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·December 18, 1998

    BARD

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJT·December 14, 1998

    ARTIFICIAL URINARY SPHINCTER

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code EZY·August 14, 1997

    AUTO SUTURE TA 90-3.5

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP·Product code GAG·April 28, 1998

    GROSHONG 9.5 FR D/L CATHETER

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code DQO·January 4, 1999