BEUDAMED
    26 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.

    FREEZER TEETHER

    FDA 510(k)
    FDA Class 2 ·Dental

    X-Trans® 22" Double Armboard

    FDA UDI
    Qfix·10841962110263·X-Trans Armboards 22” Double Armboard

    X-Trans™ 22" Double Armboard

    FDA UDI
    Qfix·10841962109632·X-Trans Armboards 22” Double Armboard

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092002066·artVeneer life upper posteriors, S, B2

    MAMMARY PROSTHESIS

    FDA Adverse Event
    MCGHAN MEDICAL CORP.·Product code FTR·May 18, 1994

    COON'S MEDIUM F-12, CATALOG NO. 200-2066

    FDA 510(k)
    FDA Class 1 ·Hematology

    Persona® Trabecular Metal®

    FDA UDI
    Zimmer, Inc.·00889024469747·

    PERSONA™ Trabecular Metal™

    FDA UDI
    Zimmer, Inc.·00889024229082·

    Persona® Trabecular Metal®

    FDA UDI
    Zimmer, Inc.·00889024469730·

    PERSONA™ Trabecular Metal™

    FDA UDI
    Zimmer, Inc.·00889024229075·

    SYNTHES (USA) LOCKING CONDYLAR PLATE (LCP) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRIMARY CARE SOLUTIONS STERILE SALINE-0.9% SODIUM CHLORIDE FOR DEVICE IRRIGATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PROMUS ELEMENT¿ PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 13, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 28, 2011

    CALAXO SCREW

    FDA Adverse Event
    Injury ·SMITH AND NEPHEW·Product code HWC·February 20, 2008

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 12, 2025

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2015

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 22, 2016

    Open Procedure Pack, part number AMS4596 Open Procedure Pack, part number AMS4596(A Open Procedure Pack, part number AMS4596(B

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017

    ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intended for use with either adult or neonatal patient populations in a hospital environment.

    FDA Enforcement
    Class II ·Terminated·Spacelabs Healthcare, Llc·February 5, 2014