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

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    PROVITEMP, DENTOTEMP, TOTALCEM, DENTOCEM

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772813841·GENUMEDI PRO SILVER SIZE IV

    HemoCue® Hb301 Analyzer

    FDA UDI
    Hemocue AB·17311091218046·HemoCue Hb301 Analyzer g/dL

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·34026704624097·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973226·

    Ascendant

    FDA UDI
    Choice Spine, LP·10885862261113·

    PRECISION PLUS TUNA OFFICE SYSTEM; PRESISION TUNA OFFICE SYSTEM; PROVU TUNA SYSTEM

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

    GIRAFFE AND PANDA WARMERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HEMOCUE HB 301 ANALYZER, MODEL 121804 AND MICROCUVETTES, MODEL 111801

    FDA 510(k)
    FDA Class 2 ·Hematology

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 3/10MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 13, 2018

    G7 SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PBI·June 2, 2017

    AVAN CMNTD SHELL SS 50MM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·April 24, 2026

    MODULAR CUP SYSTEM, RIMCUP

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    AVAN CMNTD SHELL SS 50MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 21, 2026

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    NAVIGATORTM HD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KOD·May 21, 2013

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 26, 2014

    INSYNC SENTRY

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·June 13, 2011