BEUDAMED
    9 results · 18ms · 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.

    CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT

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

    Bosworth Light Liner

    FDA UDI
    Harry J Bosworth Company·H66809214641·Soft Reline P&L Standard Kit

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123809·K-WIRE - DOUBLE TROCAR 1.4mm DIA x 100mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123793·K-WIRE - DOUBLE TROCAR 1.4mm DIA x 150mm

    CorPath GRX System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BLUE POWER FREE NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 21, 2014

    TRILOGY SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER·Product code LPH·January 9, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010