BEUDAMED
    9 results · 18ms · 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.

    SUPERSERUM REAGENT (SSR)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756370264·SINGLE DOSE EPIDURAL

    BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER

    FDA 510(k)
    FDA Class 2 ·Radiology

    AT HOME DRUG TEST, MODEL 9083 T

    FDA 510(k)
    FDA Unclassified ·Unknown

    SMR HUMERAL HEAD Ø40 MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWT·November 17, 2022

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 11, 2013

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·November 19, 2010

    ACCU-CHEK ® PERFORMA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 2, 2014

    Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 26, 2015