BEUDAMED
    32 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 ×

    SENTINEL UIBC LIQUID

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    HairCheck-DT (Amphetamines)

    FDA UDI
    Quest Diagnostics·00868586000230·HairCheck-DT (Amphetamines) is an ELISA test ki...

    NA

    FDA UDI
    Karl Storz GmbH & Co. KG·04048438008874·C-MAC S Video Laryngoscope MILLER #1

    Medstone

    FDA UDI
    Stille AB·07332339222246·Snap-on Arm Board with Pads that attaches to th...

    PANORET, MODEL 1000A

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MXD100/MX 20, OR MX 30, OR MX 40 OR MX 50--(MXD 100 SERIES)

    FDA 510(k)
    FDA Class 2 ·Radiology

    DELTA CER FEM HD 32/+3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·July 21, 2016

    BIOLOX DELTA MODULAR CERAMIC HEAD 32MM STANDARD NECK TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 18, 2016

    BIOLOX DELTA MODULAR CERAMIC HEAD 32MM STANDARD NECK TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 18, 2016

    BIOLOX DELTA MODULAR CERAMIC HEAD 32MM STANDARD NECK TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 18, 2016

    DELTA CERAMIC FEM HD DIA36/ 0MM 12/14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·August 2, 2016

    ALU FEM HD D28/+3.5/5 42/12-14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·June 17, 2016

    BIOMET BONE CEMENT R 40X1

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·January 12, 2017

    BIOLOX DELTA INSERT 36MM 54-56MM SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·June 22, 2016

    ALU FEM HEAD D32/0/5 42/12-14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·May 16, 2016

    ALU FEM HEAD D32/-4/5 42/12-14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·May 16, 2016

    TERUFLEX BLOOD BAG SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION/TERUMO BCT·Product code KSR·April 10, 2013

    ORTHADAPT BIOIMPLANT

    FDA Adverse Event
    Injury ·PEGASUS BIOLOGICS, INC.·Product code FTM·May 22, 2008

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·April 5, 2011

    BIOLOX DELTA MODULAR CERAMIC HEAD

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·August 10, 2017