BEUDAMED
    9 results · 28ms · 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.
    Filters Regulation: Us FDA ×

    WA1000

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Ultraverse® 018

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741054242·Ultraverse® 018 PTA Balloon Dilatation Catheter...

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848130240·BioMesh® 3MC - 36 x 52 mm

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M384813024US0·BioMesh® 3MC - 36 x 52 mm

    Implacil Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    SELECTIVA GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·May 15, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·October 31, 2012

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INTRAOCUL

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·August 12, 2010