BEUDAMED
    37 results · 27ms · 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 ×

    BIFIX QM

    FDA 510(k)
    FDA Class 2 ·Dental

    BD BBL¿ THIOGLYCOLLATE MEDIUM WITHOUT INDICATOR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·May 17, 2023

    C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO

    FDA 510(k)
    FDA Class 2 ·Dental

    BABY DOPPLEX 3002 (BD3002)

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    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

    BD BBL¿ THIOGLYCOLLATE MEDIUM WITHOUT INDICATOR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code JSG·May 25, 2023

    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

    BATTERY REAMER/DRILL

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code MOQ·April 16, 2013

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·March 18, 2011

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS, AB·Product code LXB·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