BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    CRYSTAL RAPID STOOL/ENTERIC ID SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110928·STERILIZING CASE SINGLE VR

    HARGIS SR2 SELF-RETRACTION SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    IMPROVED DENTAL OPERATING LIGHT

    FDA 510(k)
    FDA Class 1 ·Dental

    4.0MM COARSE DIAMOND ROUND, 16CM

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code HBE·November 22, 2021

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 23, 2013

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014

    PSS Select medical products***Biopsy Punches*** Disposable manual instrument for skin biopsy.

    FDA Enforcement
    Class II ·Terminated·Clorox Healthcare Holdings, LLC (dba HealthLink)·July 10, 2013