BEUDAMED
    41 results · 36ms · 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 ×

    REPROCESSED RESTEP COMPRESSION SLEEVES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endoscopic Injection Needle

    FDA UDI
    Carbon Medical Technologies, Inc.·00858015005943·Endoscopic Injection Needle

    andorate® 3-piece Valve Kit

    FDA UDI
    GA Health Company Limited·04897106957972·

    PTA BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ORTHOVITA PISTON SYRINGE OR IMBIBE BONE MARROW ASPIRATION SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TAPERLC BMPC LAT 6.0X132 12/14

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code KWA·August 4, 2016

    TAPERLOC PC 15.0 MM 12/14

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code KWA·August 4, 2016

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·February 27, 2026

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 25, 2022

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·May 9, 2013

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 17, 2014

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 24, 2011

    TAPERLOC COMPLETE MICROPLASTY FEMORAL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 20, 2017

    TPRLC 133 TYPE1 BM SO 11.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·September 12, 2018

    TAPERLOC BONEMASTER POROUS AND HYDROXYAPETITE COATED STEM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code KWA·May 26, 2017

    TAPERLOC TYPE1 BM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 4, 2018

    TPRLC 133 FP TYPE1 BM HO 10.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    TPRLC 133 MP TYPE1 BM HO 10.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 20, 2019

    TAPERLOC STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 19, 2017

    TAPERLOC FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 22, 2016