BEUDAMED
    7 results · 26ms · 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.

    COMPUTE RX-PLAN

    FDA 510(k)
    FDA Class 2 ·Radiology

    CIRRUS HD-OCT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Suture-TOOL System

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

    PORT-A-CATH II INTRASPINAL IMPLANTABLE ACCESS SYSTEM

    FDA Adverse Event
    Injury ·SMITHS MEDICAL MD·Product code LNY·November 19, 2012

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·February 12, 2014

    PFC PLI 8MM SZ4

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·September 29, 2010

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015