BEUDAMED
    10 results · 20ms · 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 ×

    GEN 2 Nitrile Examination Glove (Blue) With Low Dermatitis Potential Claim and with tested for use with Chemotherapy Drugs Claims

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ECHO BI-METRIC MICROPLASTY HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304698031·

    Power Dental USA

    FDA UDI
    Power Dental U.S.A. Inc.·D943193121·TISSUE PUNCH WITH GUIDE PIN 4mm x LENGTH 28.5 mm

    ECO-S

    FDA 510(k)
    FDA Class 2 ·Dental

    COMPREHENSIVE REVERSE SHOULDER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OMNIFIX®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FMF·March 6, 2026

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 4, 2015

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·October 6, 2008

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 22, 2011

    UPHOLD VAGINAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·MEDVENTURE TECHNOLOGY CORPORATION·Product code FTL·June 27, 2013