BEUDAMED
    288 results · 24ms · Sources: EU EUDAMED, US FDA

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    S40 CLINICAL ANALYZER, S TEST ALP, S TEST AMYLASE, S TEST AST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Genius Total Knee System

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215022501·

    SALINE IV FLUSH SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    THE QUIET SLEEPER

    FDA 510(k)
    FDA Class 2 ·Dental

    NOBELREPLACE CC PMC RP 4.3X10MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE USA INC·Product code DZE·June 15, 2021

    NOBELPARALLEL CC NP 3.75X13MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·March 8, 2021

    NOBELPARALLEL CC NP 3.75X13MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·March 8, 2021

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·March 12, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 28, 2011

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·July 10, 2008

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN GOLD-TITE LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026

    CERTAIN GOLD-TITE LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026