BEUDAMED
    63 results · 22ms · 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 ×

    3D SCANNER, MODEL 1230

    FDA 510(k)
    FDA Class 2 ·Radiology

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964073021·Endo Carry-On Procedure Kit

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00850038691028·

    ILT 0.014 CATHETER, MODEL C114NL2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FHC MICROTARGETING DRIVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    MOD III TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW RICHARDS FRANCE, S.A.·Product code HSH·June 25, 1997

    SILTEX SALINE MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FWM·September 21, 1998

    SILTEX SALINE

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code FWM·March 14, 1997

    SMOOTH SALINE (OVAL)

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code FWM·July 18, 1997

    SILTEX CONTOUR PROFILE

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code LCJ·July 18, 1997

    SILTEX SALINE

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code FWM·April 2, 1997

    SILTEX SALINE

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code FWM·March 20, 1997

    SILTEX LOW BLEED GEL

    FDA Adverse Event
    Injury ·MENTOR H/S, INC.·Product code FTR·June 11, 1997

    SMOOTH SALINE

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code FWM·March 20, 1997

    SILASTIC(R) MAMMARY IMPLANT, ROUND, FP

    FDA Adverse Event
    Death ·DOW CORNING CORP.·Product code FTR·September 13, 1996

    SILTEX BECKER 50

    FDA Adverse Event
    Injury ·MENTOR H/S, INC.·Product code FTR·June 11, 1997

    SILTEX SALINE

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code FWM·June 11, 1997

    SILTEX SALINE

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code FWM·July 18, 1997

    SILTEX LOW BLEED GEL

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code FTR·July 18, 1997

    SPECTRUM CONTOUR POST-OP ADJUSTABLE

    FDA Adverse Event
    Injury ·MENTOR H/S, INC.·Product code LCJ·June 11, 1997