BEUDAMED
    324 results · 29ms · Sources: EU EUDAMED, US FDA

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    KAIYANG ALUMINUM WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Removalon

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·00348783003857·REMOVALON I DRY PK SINGLE

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964073045·The ENDO CARRY-ON Procedure Kit contains all of...

    METRONIC SOFAMOR DANEK CEMENT RESTRICTOR

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

    1ML UNITRACT 27G X 1/2 TUBERCULIN SYRINGE, MODEL 132BY2-1

    FDA 510(k)
    FDA Class 2 ·General Hospital

    *

    FDA Adverse Event
    Malfunction ·DOW CORNING CORP/ MEDICAL PRODUCTS·Product code FEW·March 23, 1998

    INTRA-AORTIC BALLOON PUMP

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·June 19, 1998

    INTRA-AORTIC BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·June 19, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 22, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 22, 1998

    SOFTFORM FACIAL IMPLANT

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

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 8, 1998

    STAT DL 9.5 FR. 34 CC. IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORP·Product code DSP·July 9, 1998

    STAT DL 9.5 FR. 40CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 14, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 22, 1998

    STAT DL 10.5 FR. 50 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 8, 1998

    *

    FDA Adverse Event
    Product code FRN·May 30, 1997

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 22, 1998

    *

    FDA Adverse Event
    Malfunction ·*·Product code GAG·December 31, 1997

    ATLANTIS CANCELLOUS SCREW

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MANUFACTURING·Product code KWQ·January 4, 1999