BEUDAMED
    13 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.

    60 FUNDUS CAMERA CF-60UV

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Stern EX Acid Etched Implant RP 3.75x13.0mm, Biomain, Ti

    FDA UDI
    STERNGOLD DENTAL LLC·00841549109201·The Sterngold Acid Etch Dental Implant System c...

    Map-iT

    FDA UDI
    ACCESS POINT TECHNOLOGIES, INC.·00818083015480·Fixed, 10 electrode, MPB, 5-5-5-24-3-3-3-3-3mm ...

    DISPOSABLE HYPODERMIC NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KANEKA PHARMA AMERICA XPRESS-WAY RX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 30, 2014

    TI PANGEA(TM) LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code NKB·January 8, 2013

    HUBER NEEDLE EXTENSION SETWITH INTERLINK Y

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·November 17, 2010

    THROMBUSTER II

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code MMY·March 17, 2014

    THROMBUSTER II

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code DXE·October 23, 2012

    THROMBUSTER II

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code DXE·December 21, 2012

    THROMBUSTER II

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code DXE·January 16, 2019

    ROADRUNNER THE FIRM HYDROPHILIC WIRE GUIDE

    FDA Adverse Event
    Injury ·COOK INC·Product code DQX·January 26, 2018