BEUDAMED
    36 results · 23ms · Sources: EU EUDAMED, US FDA

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    Getinge GSS610N Series Steam Sterilizer

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DJO SURGICAL

    FDA UDI
    Encore Medical, L.P.·00190446923107·SPECIAL EMPOWR KNEE 2 DEG VARUS, TIBIAL RECUT G...

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG

    PLATELET CONCENTRATE SEPARATION KIT FOR CELSEP CENTRIFUGE SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    VECTRA (TM) VASCULAR ACCESS GRAFT-5MM DIAMETER,6MM DIAMETER AND VECTRA (TM) VASCULAR ACCESS GRAFT FOR REVISION-5MM DIAME

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TALENT TAA STENT GRAFT

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·May 9, 2019

    TALENT TAA STENT GRAFT

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·May 9, 2019

    AXIOM REG IMPLANT

    FDA Adverse Event
    Injury ·ANTHOGYR·Product code DZE·September 10, 2019

    AXIOM REG IMPLANT

    FDA Adverse Event
    Injury ·ANTHOGYR·Product code DZE·September 11, 2019

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    PINGHU WEIFENG MATERIAL TECHNOLOGY·Product code IKX·October 27, 2014

    PROTECTA XT CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·August 11, 2011

    DELTA CER HEAD 12/14 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LZO·July 2, 2013

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·January 15, 2013

    COBAS 6000 E 601 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 17, 2019

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·January 2, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 4, 2013

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 3, 2020

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 3, 2020

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 3, 2020

    UNKNOWN KNEE FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 3, 2020