BEUDAMED
    12 results · 20ms · 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 ×

    ALOCLAIR ORAL GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    Cortera

    FDA UDI
    Xtant Medical Holdings, Inc.·00840311210558·Tap, Cann, Jacobs, 9.5

    Vantage

    FDA UDI
    Exactech, Inc.·10885862605733·

    NA

    FDA UDI
    Summit Medical, Inc.·00385640001212·

    EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CYPRESS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·August 16, 2021

    REDUCTION FORCEPS WITH POINTS RATCHET 174MM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTD·April 8, 2013

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·March 23, 2011

    ACCU-CHEK INFORM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·May 2, 2008

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012

    The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018