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

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    MODEL CF-300 THREE CHANNEL FLOW METER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BR2000 BLADES

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919100744·K7-2190-39F

    BR2000 BLADES

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919100751·K7-2190-47F

    SYNTHES DISTRACTION OSTEOGENESIS SYSTEM, MR CONDITIONAL WITH EXPANDED INDICATIONS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Solax Electric Scooter

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SUPREME EP CATHETER 5F, QUADRIPOLAR, JSN

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DRF·August 5, 2009

    X-FLOW PROSTATECTOMY CATHETER

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code EZL·October 8, 2024

    SMARTLIFE LARGE ASEPTIC HOUSING

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS, INSTRUMENTS DIV.·Product code HWE·April 8, 2014

    SWARTZ BRAIDED TRANS. GUIDING INT., 8F, LAMP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DYB·October 11, 2012

    PROXIMATE** PLUS MD MULTI-DIRECTIONAL RELEASE SKIN STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDT·August 10, 2010