BEUDAMED
    9 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.
    Filters Regulation: Us FDA ×

    MEDISYSTEMS BUTTONHOLE NEEDLE SETS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PED NIH™ Cardio-Marker

    FDA UDI
    MEDTRONIC, INC.·00613994964168·WVN CATH 990803 5PK 6F 65CM PED NIH

    PED NIH™ Cardio-Marker

    FDA UDI
    MEDTRONIC, INC.·00763000200206·WVN CATH 990803 5PK 6F 65CM PED NIH

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556812228·VERSION ROD

    SYRINGE TONOMETER

    FDA 510(k)

    HANSON MEDICAL FACIAL IMPLANTS

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

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 5, 2013

    UNKNOWN ZIMMER SHOULDER

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HSD·February 8, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014