BEUDAMED
    10 results · 21ms · 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 ×

    BB-613-BPM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704265255·

    NA

    FDA UDI
    SYNTHES (U.S.A.) LP·10886982165657·3.5MM CLAVICLE HOOK PLATE 8 HOLES RIGHT-15MM HO...

    2.0/2.4MM FRACTURE SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036036003·

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517083316·

    ENSEAL X1 Tissue Sealer, Curved Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue Sealer, Curved Jaw, 37 cm Shaft Length, ENSEAL X1 Tissue Sealer, Curved Jaw, 45 cm Shaft Length

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

    ENCORE REVERSE SHOULDER PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CRE(TM) BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KOG·September 9, 2011

    TAXUS EXPRESS2 ATOM PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·November 20, 2008

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 18, 2013