BEUDAMED
    26 results · 21ms · 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 ×

    OWL RF INSULATED CANNULAE

    FDA 510(k)
    FDA Class 2 ·Neurology

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486004330·MCK ONLAY INSERT TRIAL (SIZE 8 X 10mm)

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486004385·MCK ONLAY INSERT TRIAL (SIZE 8 X 15mm)

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486004378·MCK ONLAY INSERT TRIAL (SIZE 8 X 14mm)

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486004323·MCK ONLAY INSERT TRIAL (SIZE 8 X 9mm)

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486004347·MCK ONLAY INSERT TRIAL (SIZE 8 X 11mm)

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486004354·MCK ONLAY INSERT TRIAL (SIZE 8 X 12mm)

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486004316·MCK ONLAY INSERT TRIAL (SIZE 8 X 8mm)

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486004392·MCK ONLAY INSERT TRIAL (SIZE 8 X 16mm)

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486004361·MCK ONLAY INSERT TRIAL (SIZE 8 X 13mm)

    PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OLYMPUS FT4-FREE THYROXINE, OLYMPUS T4- TOTAL THYROXINE, MODEL# OSR210102, OSR210104

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·July 12, 2011

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code LFR·June 14, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code EZW·September 16, 2008

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·July 18, 2019

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·June 17, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 8, 2019

    KIT BD MAX EXT ENTERIC BACTERIAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code PCH·June 21, 2022

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·January 23, 2019