BEUDAMED
    3,124 results · 35ms · 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 ×

    DIC TRACHEOSTOMY TUBE AND PORTEX BLUE LINE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    addition Junior/DIC 4 x 50 ml

    FDA UDI
    DETAX GmbH·EDET041601·

    addition Junior/DIC 2 x 50 ml

    FDA UDI
    DETAX GmbH·EDET041591·

    OTOSONIC (OSI) LPS D; LPS D IC; LPS D ASP

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    ABSORBABLE GELATIN

    FDA Adverse Event
    Injury ·PFIZER, INC.·Product code LMF·August 31, 2020

    Edge™ Diamond DIC-016C Double Inverted Cone

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172007900·Diamond dental bur, reusable

    Edge™ Diamond DIC-016C Double Inverted Cone

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172007917·Diamond dental bur, reusable

    DIC

    FDA Adverse Event
    Injury ·DALTON MEDICAL·Product code ITJ·October 18, 2010

    MALLINCKRODT

    FDA Adverse Event
    Malfunction ·JUAREZ HENEQUEN·Product code BTO·August 16, 2007

    DIC LARYNGECTOMY; DIC TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·NULL·Product code BTO·September 24, 2022

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·February 24, 2014

    CONTACT DETACH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 10, 2025

    TALENT THORACIC STENT GRAFT SYSTEM - COILTRAC

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·September 1, 2010

    TALENT THORACIC STENT GRAFT SYSTEM - COILTRAC

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·September 1, 2010

    TALENT THORACIC STENT GRAFT SYSTEM - COILTRAC

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·September 1, 2010

    SHILEY DESPOSABLE INNER CANNULA

    FDA Adverse Event
    Malfunction ·MALLINCKRODT, INC.·Product code BTO·May 21, 2001

    ULTRAFLUX EMIC2

    FDA Adverse Event
    Injury ·ST. WENDEL AG·Product code FJK·July 6, 2023

    GOLD HEMOSHIELD

    FDA Adverse Event
    Death ·MEADEX COMPANY·Product code DSY·May 23, 2002

    SHIELY, DISPOSABLE SIZE 6, EXACT PRODUCT TYPE UNKNOWN

    FDA Adverse Event
    Death ·MALLINCKRODT INC.·Product code BTO·March 19, 2002

    FLOSEAL

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - HAYWARD·Product code LMF·October 10, 2018