BEUDAMED
    7 results · 17ms · 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.

    SHELHIGH NO-REACT VASCUPATCH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PE/Dazzle™ 594 anti-human CD13

    FDA UDI
    BIOLEGEND, INC.·00810034702272·URL: https://www.biolegend.com/en-us/products/p...

    ARTHREX BIO-COMPOSITE SUTURE ANCHORS: ARTHREX BIO-COMPOSITE PUSHLOCK, BIO-COMPOSITE TAK AND BIO-COMPOSITE CORKSCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Distal Radius Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 28, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 9, 2011

    MEDTRONIC RESOLUTE STENT

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code NIQ·July 24, 2014