BEUDAMED
    85 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.

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·FX MINIRAIL RX PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) CATHETER

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·FX MINIRAIL PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) CATHETER

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·FX MINIRAIL RX PTCA CATHETER

    Affiniti™

    FDA UDI
    TORNIER, INC.·00846832001958·

    Promolux Polymer H-pink

    FDA UDI
    Merz Dental GmbH·D7091020037·Promolux Polymer H-pink, 1000g

    AOS SMALL BONE REAMER Ø3.7 x 328mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665028867·

    ROSA POLYAXIAL REFERENCE SIZE 3

    FDA UDI
    Orthosoft Inc·00889024674776·

    DRIED GRAM NEGATIVE MIC/COMBO PANELS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    GORE VIABAHN ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code PFV·March 25, 2021

    Stent, Renal

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC AVE BRIDGE EXTRA SUPPORT OVER THE WIRE RENAL STENT SYSTEM

    Heart-Valve, Mechanical

    FDA Pre-Market Approval
    FDA Class 3 ·ON-X (R) PROSTHETIC HEART VALVE, MODEL ONXA

    GORE VIABAHN ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code PFV·August 6, 2020

    ON-X PROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·ON-X LIFE TEHCNOLOGIES, INC.·Product code DYE·January 14, 2016

    ON-X MITRAL PROSTHETIC HEART VALVE

    FDA Adverse Event
    Other ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·July 14, 2011

    VALIANT CAPTIVIA THORACIC STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·March 25, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·March 12, 2014

    IN TOUCH ZU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·March 9, 2011

    VNGD ANT STBLZD BRG 10X79

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 14, 2020

    ONX AORTIC ANATOMIC EXT 27/29

    FDA Adverse Event
    Injury ·ONX LIFE TECHNOLOGIES, INC.·Product code LWQ·March 14, 2017

    Heart-Valve, Mechanical

    FDA Pre-Market Approval
    FDA Class 3 ·ON-X PROSTHETIC HEART VALVE