BEUDAMED
    27 results · 24ms · 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 ×

    HARDYDISK CEFONICID, 30 MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Preat

    FDA UDI
    Preat Corporation·00842092183908·ASC Straumann? BL RC-compatible Engaging Titani...

    Premier

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·D6913001490·COMP CORE AF AUTO-CURE TWIST-WHITE

    GRADIA®

    FDA UDI
    Gc America Inc.·14548161392815·GRADIA® TRANSLUCENT T1

    GRADIA®

    FDA UDI
    Gc America Inc.·D0470014901·GRADIA® TRANSLUCENT T1

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001490·artVeneer life lower anteriors, UBIM, D3

    CYNOSURE PHOTOGENICA VLS-STAR

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

    METHAFILCON A

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BD SYRINGE 3ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 7, 2025

    SYSTEM 9 LARGE ASEPTIC HOUSING

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code HWE·January 22, 2024

    FACE TENT

    FDA Adverse Event
    Malfunction ·UNOMEDICAL S.A. DE C.V.·Product code BYG·November 19, 2010

    VENTAK CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Death ·CARDIAC PACEMAKERS, INC.·Product code LWS·October 7, 1993

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·July 9, 2018

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 5, 2013

    UROLOGICAL BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code EZN·February 25, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·February 19, 2008

    BD SYRINGE 5ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 7, 2025

    BD SYRINGE 1ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 7, 2025

    First Breath Adult Face Tent (Non-latex) 50/CA Reorder Number: 001490 Face Tent Is a special type of aerosol mask used when the delivery of oxygen is not the primary objective. Normally this type of mask is used to deliver an aerosol mist to cool and moisturize the nasal passages or sinuses after surgery

    FDA Recall
    Terminated ·Smiths Medical Hythe Hythe, Kent United Kingdom·Product code BYG·February 11, 2011

    Face Tent Hospilak Ref. No. 110-E, Face Tent, Adult No Tubing, Manufactured for Unomedical inc. Hospilak Ref. No. 111-E, Face Tent, Adult No Tubing, with 15mm OD Connector Manufactured for Unomedical inc. Hospilak Ref. No. 115-E, Face Tent, Adult 5 (1.5m) Tubing Manufactured for Unomedical inc. Hospilak Ref. No. 116-E, Face Tent, Adult 6 (1.8 m) Aerosol Tubing Manufactured for Unomedical inc. McKesson Aerosol Mask, Face Tent Adult, No Tubing Reorder No. 86-110E Face Tent Adult, 6 (1.8m) Aerosol Tubing Reorder no. 86-116E Smiths Medical Portex First Breath Adult Face Tent (Non-latex) Ref 001490 Smiths Medical Portex First Breath Adult Face Tent with Tubing, 188cm (5 ft.) (Non-latex) Ref 001492 Owens & Minor MediChoice Adult Face Tent Re-Order #RSP3000 and Face Tent, Adult 6 (1.8m) Aerosol Tubing Re-Order #RSP3060

    FDA Recall
    Terminated ·Convatec Inc.·Product code BYL·January 7, 2011