BEUDAMED
    35 results · 29ms · 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 ×

    FASTIN RC ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70606641·Sprint II Brackets Roth .022" 400 Brackets 3-5 ...

    COPELAND RESURFACING HUMERAL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VIGILANCE CCO/CEDV & VIGILANCE CCO/SVO2/CEDV MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TESS HUM INSERT TH 6 DIA36 S1

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·March 7, 2017

    TESS HUMERAL INSERT TH 8 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

    TESS HUMERAL REVERSED INLAY 036 S1 12MM

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 9, 2017

    TESS HUMERAL INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

    CUSTOM REVERSE HUMERAL LINER

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 27, 2017

    TESS GLEN BASEPLATE S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·May 25, 2016

    TESS HUMERAL REVERSE COROLLA S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·November 18, 2016

    UNKNOWN TESS GLENOID COMPONENT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·July 7, 2017

    TESS HUM INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·May 10, 2017

    UNKNOWN TESS HUMERAL INSERT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·June 1, 2017

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·March 27, 2013

    MBT CEM KEEL TIB TRAY SZ3

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code NJL·April 6, 2011

    STARCLOSE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·June 13, 2008

    TESS HUMERAL INSERT TH 8 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 17, 2017

    TESS HUMERAL INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·January 25, 2017

    TESS HUM INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 6, 2017