BEUDAMED
    34 results · 23ms · Sources: EU EUDAMED, US FDA

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    ORTHOLOC™ 2 Lapidus with Rotation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327627213·Mako Shoulder Burr

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306822919·Killian (Von Eicken) Antrum Cannula - 3mm Bulbou

    MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    S-SCAN, MODEL 9800020010

    FDA 510(k)
    FDA Class 2 ·Radiology

    BIOLOX DELTA CER LNR 36MM E

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

    RINGLOC-X E1 H/W 56/36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·April 27, 2026

    BIOLOX DELTA CER LNR 40MM G

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·April 27, 2026

    PD2000 ADVISORY

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 3, 2008

    SECURE 3 MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 29, 2011

    CVC KIT: 2-LUMEN 7 FR X 16 CM

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code FOZ·June 24, 2013

    REVOLUTION (ASSEMBLED INTO CUSTOMISED PERFUSION TUBING)

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code KFM·December 11, 2025

    AVAN E1 INSERT 28 S 52

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·March 6, 2025

    BIOLOX DELTA CER LNR 32MM E

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·September 8, 2025

    RINGLOC BIPOLAR VIVACIT-E

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·September 10, 2025

    INSPIRE 7M HOLLOW FIBER OXYGENATOR, INSPIRE 7 DUAL HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·June 14, 2019

    REVOLUTION CENTRIFUGAL BLOOD PUMP COATED

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code KFM·November 11, 2024

    REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC COATING

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code KFM·December 2, 2022

    REVOLUTION PHISIO CENTRIFUGAL PUMP

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code KFM·June 23, 2021

    REVOLUTION PHISIO CENTRIFUGAL PUMP

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code KFM·May 20, 2021