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

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    HEMESPEC CHECK SET

    FDA 510(k)
    FDA Class 2 ·Hematology

    SCANLAN® Retractors

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159013092·1 each blade for Pediatric Titanium Retractor, ...

    KSEA ELECTRONIC CO2 ENDOFLATOR LC, MODEL 26430320-1

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

    RENEW NEUROSTIMULATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    COMP LK SCR 3.5HEX 4.75X30 ST

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·May 8, 2014

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 18, 2012

    PFC SIG MOD TIB TRAY CEM SZ2.5

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code JWH·August 10, 2010

    Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box

    FDA Recall
    Terminated ·Mueller Sports Medicine, Inc·Product code ITQ·June 18, 2020

    Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021