BEUDAMED
    23 results · 25ms · Sources: EU EUDAMED, US FDA

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    AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517636911·CoRoent Ant TLIF PEEK, 13x10x34mm 15°

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169604797·SPACER 2130345 OLIF25 27MM 0 DEG 12X45

    ArgenZ HT+ 98x16 ML D3B

    FDA UDI
    ARGEN CORPORATION, THE·D818130345·Dental porcelain/ceramic restoration kit

    ABC

    FDA UDI
    Conmed Corporation·10653405002604·ABC HANDPIECE 45° Footswitching Handpiece

    PRINCETON

    FDA UDI
    Princeton Medical Group, Inc.·00810158219670·SUCTION TUBE HOUSE 4.5MM X 2.0MMØ 3.5"

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529585037·Apex Tibial Nail Ø 13 x 345mm

    SYSTEMS INTEGRATION MODEL: ENDOALPHA

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BREATHE TECHNOLOGIES VENTILATOR AND ACCESSORIES (BT-V2S)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SET, ADMINISTRATION, INTRAVASCULAR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2016

    Truliant

    FDA UDI
    Exactech, Inc.·10885862314703·

    THREE PEG PATELLA 35MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 7, 2024

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·May 9, 2011

    ADVANTA 2 BED

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FNL·March 9, 2013

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 22, 2008

    STOPCOCK MANIFOLD GANGS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FMG·June 17, 2020

    TRULIANT TIB IMP CR INS STD SZ 4.5, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 7, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 2, 2025

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 15, 2024

    TRULIANT TIB IMP CRC INSERT SZ 4.5, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 20, 2022