BEUDAMED
    11 results · 19ms · 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 ×

    SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    LIQUID ASSAYED MULTIQUAL CONTROL LEVEL1 #981600; LEVEL 2 #981700; LEVEL 3 #981800

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    JEDMED

    FDA UDI
    JEDMED INSTRUMENT COMPANY·M6339818000·VDC LOUPE SYSTEM W/LED 28MM PD

    JEDMED

    FDA UDI
    JEDMED INSTRUMENT COMPANY·M633981800T0·VDC LOUPE SYSTEM TITANIUM 28MM ##

    T12S TELEMETRY TRANSMITTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRIP, HOSPITAL UTILITY

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ACCU-CHEK SENSOR COMFORT TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code NBW·August 10, 2006

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 1, 2020

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 27, 2013

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 8, 2011

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 5, 2014