BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    PRECICE Intramedullary Limb Lengthening System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171028826·PESSARY, MARLAND #4, W/O SUPPORT, 2.75"

    AMSINO SUTURE REMOVAL KIT

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

    COMPRESSIBLE LIMB THERAPY SYSTEM MODEL WHF-324 (POWER-Q1000 PLUS)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    COCR HEAD 28/ 0 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LPH·June 20, 2023

    VIRTUOSO VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 6, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 14, 2015

    TREVO XP PROVUE 4MM X 30MM

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code NRY·July 24, 2020

    AVAN REINF RING SS 48/58MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 29, 2025