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 ×

    APILUS ELECTROPIL

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

    COUNTERBALANCED VERTICAL CASSETTE HOLDER

    FDA 510(k)
    FDA Class 1 ·Radiology

    ViaOne Epicardial Access System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESOLUTE INTEGRITY RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·December 1, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·February 5, 2013

    M2A-TAPER LINER SZ 41/32

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDL·July 18, 2014

    TPRLC 133 MP TYPE1 PPS HO 17.0

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·January 22, 2020

    TPRLC 133 T1 PPS HO 15X150MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·January 22, 2020

    TPRLC 133 MP TYPE1 PPS HO 16.0

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·January 22, 2020

    TPRLC XR MP T1 PPS 15X115MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·January 22, 2020