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

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    E.Z. LOCK WHEELCHAIR RESTRAINT DEVICE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DISPOSABLE MANIFOLD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CANAL WALL PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    2.0 LACTOSORB SYSTEM L-SHAPE PLATE - LEFT EXTENDED

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·January 31, 2022

    LACTO SCR 2.0X7MM 2.0 SYS 2/PK

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·January 31, 2022

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 25, 2014

    KINETIX PLUS PTCA GUIDEWIRE

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·November 10, 2010

    CADD-PRIZM VIP AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC)·Product code MEA·January 11, 2008

    BIOMET StageOne Knee Femoral Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 432165.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020