BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    DG 200/300 DIGITAL ANGIOGRAPHIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Jaeger

    FDA UDI
    Jaeger Medical GmbH·14250892902491·Adapter, ID 30 mm to ID 30 mm

    Vyaire

    FDA UDI
    Jaeger Medical GmbH·14250892904266·Adapter, ID 30 mm to ID 30 mm

    Jaeger

    FDA UDI
    Jaeger Medical GmbH·14250892908127·Adapter, ID 30 mm to ID 30 mm

    Endo-Model SL Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575384129·Modular Stem, with male taper for 6mm noses, ce...

    Z-CHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SeraQuest HSV Type 2 Specific IgG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KWA·June 5, 2014

    SPINBRUSH PROCLEAN POWERED TOOTHBRUSH

    FDA Adverse Event
    Malfunction ·CHURCH & DWIGHT CO., INC.·Product code JEQ·November 13, 2012

    LANDMARX EVOLUTION

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION·Product code HAW·September 29, 2010

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

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