BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    STERiJECT Low Dead Space, STERiJECT The Invisible Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD BBL™ Taxo™ Differentiation Discs for Nitrate

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902317340·BD BBL™ Taxo™ Differentiation Discs for Nitrate

    LOCKING SCREW, FULLY THREADED 5X45 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 30, 2009

    ALL-BOND UNIVERSAL SC (NOT FINALIZED)

    FDA 510(k)
    FDA Class 2 ·Dental

    GENERATION 4 POLISHED FEMORAL HIP PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTSTART SLA BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DQA·October 14, 2014

    INFUSO.R.

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 1, 2011

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 17, 2013

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022