BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    DEPUY ACE TROCHANTERIC SIDE PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970503·anteriors; shade BL2; mould BIL

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111331183·CURETTE EXCA W/O HOLE 1MM

    EIT Cellular Titanium Cervical Cage, EIT Cellular Titanium PLIF Cages, EIT Cellular Titanium TLIF Cages, and EIT Cellular Titanium ALIF Cages

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LOUISVILLE CLAMP PRODUCT #65-172

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LOGIC CR TIB INSERT SLOPE ++, SZ 3.5, 9 MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·May 17, 2024

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 20, 2013

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·January 19, 2011

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 10, 2014

    T-HANDLE INSERTER

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·April 29, 2021

    T-HANDLE

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code LXH·May 2, 2023

    IMPLANT INSERTER SH CONNECTION

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·May 2, 2023