BEUDAMED
    278 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 ×

    Ice Cooling IPL Hair Removal Device (UI20 DB, UI20 RE, UI20 GP, UI20 PW, UI20S DB, UI20S RE, UI20S PW, UI20S GP,UI20 WH, UI20 GR, UI20 BS, UI20 MP, UI20 BL, UI20 PN, UI20 BR, UI20WG, UI20S WH, UI20S GR, UI20S BS, UI20S MP)

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

    SAMA DISPOSABLE BLOOD PRESSURE CUFF BARRIERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PHACO CHOP NEEDLES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    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·August 20, 1999

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 29, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·July 10, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLGIES, INC.·Product code FTL·January 20, 1999

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORP.·Product code DSP·October 10, 1998

    MITYVAC

    FDA Adverse Event
    Malfunction ·PRISTECH, INC.·Product code HDB·July 8, 1998

    INTRA-AORTIC BALLOON CATHETER

    FDA Adverse Event
    Injury ·DATASCOPE CORPORATION·Product code DSP·January 13, 1999

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORP.·Product code DSP·September 16, 1998

    STAT DL 9.5 FR. 34 CC. IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORPORATION·Product code DSP·January 13, 1999

    WRIGHT

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL·Product code LZO·September 17, 1998

    RESTORE 3.75X10 SELF-TAPPING IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·August 7, 1998

    SHILEY DISPOSABLE CANNULA CUFFLESS FENESTRATED TRACHEOSTOMY

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL, INC.·Product code BTO·March 16, 1998

    SOFTFORM FACIAL IMPLANT

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

    RESTORE 3.75X10 SELF-TAPPING IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 22, 1998

    RESTORE 4X10 TPS SCREW

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

    SERIES TEN THOUSAND MASTER

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·July 24, 1998