BEUDAMED
    21 results · 22ms · Sources: EU EUDAMED, US FDA

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    NIOX VERO Airway Inflammation Monitor

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HHM

    FDA UDI
    Oticon A/S·05707131286086·H160V2 TI, RITE 312 WL SGR HHM

    LOCKHART MUMMERY PROBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896017498·LOCKHART MUMMERY FISTULA PROBE HOOK EYE HOLE TI...

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768L15023318K0·Tap

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768L15023313K0·Tap

    Ligament Balancing Block

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215074029·

    JMS SYSLOC A.V.FISTULA NEEDLE SET

    FDA UDI
    JMS SINGAPORE PTE LTD·08888483005406·SYSLOC AVF 15GX11/4" BE 30CM W/CLAMP

    OMRON NON-INVASIVE BLOOD PRESSURE MONITOR WITH AUGMENTATION INDEX, MODEL HEM-9000AI

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SUDOSCAN

    FDA 510(k)
    FDA Class 2 ·Neurology

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·January 7, 2016

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    6000CMS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 29, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORP·Product code LGW·September 3, 2008

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·June 10, 2011

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    UNK ATTUNE KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code JWH·July 11, 2022

    UNK ATTUNE KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code JWH·July 11, 2022

    VITAL-PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·May 24, 2016

    UNK ATTUNE KNEE PATELLA

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code JWH·July 11, 2022