BEUDAMED
    8 results · 19ms · 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 ×

    MODIFICATION OF PROLENE (POLYPROPYLENE) HERNIA SYSTEM, NONABSORBABLE SYNTHETIC SURGICAL MESH

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

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984220·anteriors; shade A4; mould 98

    HOUTS HYSTERECTOMY DRAIN

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

    AIR WATER SYRINGE TIP SHIELD

    FDA 510(k)
    FDA Class 1 ·Dental

    AT HOME DRUG TEST PHARATECH

    FDA Adverse Event
    PHAMATECH·Product code MVO·September 24, 2003

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013

    LOW PROFILE SELF TAPPING BONE SCREW 6.5MM X 25MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·February 10, 2011

    UNKNOWN DEPUY METAGLENE

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code HSD·August 6, 2014