BEUDAMED
    8 results · 20ms · 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 ×

    CUPRALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    DirectLink ICP Module, DirectLink ICP Extension Cable, Patient Monitor Interface Cables

    FDA 510(k)
    FDA Class 2 ·Neurology

    STAXX XD SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INTRAOCUL

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·January 4, 2011

    PERFUSOR SPACE ACM-KIT

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·July 17, 2014

    VANGUARD CR ILOK FEM-LT 65

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 21, 2021

    BIOMET CC CRUCIATE TRAY 71MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 21, 2021