BEUDAMED
    7 results · 20ms · 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.

    PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TRYPTIC SOY BROTH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    H.R. JAKOBI SURG. INSTRUMENTS #9-SEC.48

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

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 19, 2014

    TRIDENT 0 DEG INSERT 36MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·October 21, 2010

    NON-POWERED TRACTION APPARATUS AND ACCESSORIES

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code HST·December 22, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021