BEUDAMED
    14 results · 30ms · 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 ×

    PAL Infiltration System

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

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113318·PHACO KNIFE 1.8MM ANGLED (BX/5)

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113195·PS Insert, Size 3 x 18mm

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306824456·Walther Female Dilator-Catheters 13cm, 18Fr

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676220318070·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676220318000·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676220318150·

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 15, 2022

    VIVI ERGON-X HF

    FDA 510(k)
    FDA Class 2 ·Dental

    SCIVOLUTIONS VARIOUS ANTIBACTERIAL BANDAGES

    FDA 510(k)
    FDA Unclassified ·Unknown

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 3, 2014

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 23, 2011

    FORTIFY ASSURA VR, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 11, 2013

    NI

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·February 20, 2024