BEUDAMED
    35 results · 23ms · 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 ×

    Thermoforming Sheet Materials

    FDA 510(k)
    FDA Unclassified ·Unknown

    DEBAKEY THORACIC BAYONET FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896092914·DEBAKEY THORACIC BAYONET FORCEPS

    Retraction Drill Guide

    FDA UDI
    Treace Medical Concepts, Inc.·00810111222112·Retraction Drill Guide

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776302931·Parker-Mott Retractor

    Tissue Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112847·BARRON ARTIFICIAL ANTERIOR CHAMBER

    STILLE Scissors

    FDA UDI
    Stille AB·07332339201333·STILLE VASCULAR SUPERCUT SCISSORS 125° 17 cm 6....

    VISION SCIENCES FLEXIBLE ENT SCOPE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    JET PORT PLUS CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COMPRESSURE FRACTURE REPAIR IMPLANT

    FDA Adverse Event
    Injury ·USI ORTHOPAEDICS LLC DBA U.S. ORTHOPAEDICS·Product code HTN·April 6, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 1, 2016

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 15, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 1, 2013

    ESPRIT VENTILATOR, Model V1000

    FDA Recall
    Terminated ·Respironics California Inc·Product code CPK·June 8, 2001

    HOLDING SLEEVE-LONG FOR MATRIX

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·December 21, 2016

    GENTLE CATH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL S.R.O.·Product code GBM·October 7, 2020

    L3C3850 - GENTLECATH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL S.R.O.·Product code KOD·January 21, 2021

    L3C3850 - GENTLECATH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL S.R.O.·Product code KOD·January 21, 2021

    L3C3850 - GENTLECATH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL S.R.O.·Product code KOD·January 21, 2021

    L3C3850 - GENTLECATH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL S.R.O.·Product code KOD·January 21, 2021