BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    AT HOME DRUG TEST, MODEL 9078

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    AT HOME DRUG TEST PHARATECH

    FDA Adverse Event
    PHAMATECH·Product code MVO·September 24, 2003

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197775·AK3 PS-C Insert Trial Size 2, 20mm

    HOUTS HYSTERECTOMY DRAIN

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SYNCHRON CX4-CE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    BIOLOX DELTA CER LNR 36MM F

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 24, 2024

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·March 8, 2013

    INTEGRATED APD SET W/CASSETTE3 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 17, 2011

    ACUDOSE-RX

    FDA Adverse Event
    Malfunction ·AESYNT INCORPORATED·Product code BRY·July 24, 2014

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Right, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-32, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-33, c) 44, 47, 50, 53 head, Large, Item Number 314-13-34, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-35; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024