BEUDAMED
    22 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 ×

    AMNISCREEN HOME DETECTION LINER KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DP-REPAIR

    FDA UDI
    Denplus Inc·D8451071100·DP-REPAIR-F, CLR, 454 g

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702407679·Elvarex 2/Knee High/Slant-Open Toe/Dotted 5 cm ...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702366464·ELVAREX 3/KNEE HIGH/OPEN TOE/DOTTED 2,5 CM SILI...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702542653·Elvarex Forte 3/Knee High/Profile-Slant-Closed ...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702519242·Elvarex 3/Chap Style/Closed Toe, E-Version, Kne...

    Bone Screws

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132134405·7.0 CANNULATED SCREW SET (IMPLANT, INSTRUMENT, ...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702545722·ELVAREX FORTE 3/THIGH HIGH/SLANT-CLOSED TOE/DOT...

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K0171000·Implant Remover

    MATIRA ANTERIOR CERVICAL SYSTEM

    FDA UDI
    Kalitec Direct LLC·B07307K0171000·Driver, Temporary Pin

    300 PV COMPLETE ELECTROTHERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BIOZ.COM HEMODYNAMIC MONITOR WITH BIOZ TECT SENSOR AND BIOZ TECT CABLE IMPEDANCE PLETHYSMOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MetaSystems Probes

    FDA UDI
    MetaSystems Probes GmbH·04251315818286·XL CCND1, Break Apart Probe

    ARTEFILL DERMAL FILLER

    FDA Adverse Event
    Injury ·SUNEVA MEDICAL, INC.·Product code LMH·January 10, 2019

    HATCP STEM POR TIB PLT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·March 5, 2024

    LINEAR 3-6

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 3, 2020

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 5, 2024

    RESTORE SENSOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 22, 2013

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·July 10, 2008

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 27, 2011