BEUDAMED
    19 results · 25ms · Sources: EU EUDAMED, US FDA

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    BARD PERFIX LIGHT PLUG, MODELS 0117050, 0117060, 0117070, 0117080, 0117150, 0117160

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

    DELTA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613252598190·S-DRILLING TAP, HEX, FOR 4mm SCREW

    C02 LASER MULTIPULSE

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

    FIRST SPEP

    FDA 510(k)
    FDA Class 2 ·Dental

    APHIS PLATEAU RADIAL T1

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JWJ·May 19, 2017

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 3, 2013

    PINN CAN BONE SCREW 6.5MMX30MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS 121965·Product code NDJ·September 16, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 18, 2011

    LOCKSCR F/NAILS Ø5 L86 XL25

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code JDS·September 12, 2023

    PFNA-II BLADE L85 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HSB·September 22, 2023

    TIBIAL NAIL ADVANCED Ø10 L315

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDS·June 8, 2023

    2.0MM TI VA-LCKNG SCR SLF-TPNG WITH T6 STARDRIVE RECESS 10MM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·April 25, 2023

    CRANIAL-SCR PLUSDRIVE Ø1.6 SELF-DRILL L4

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JEY·June 22, 2023

    PL 1-HO F/FEM NECK SYST TAN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code KTT·June 19, 2023

    TIBIAL NAIL-ADVANCED / 10MM 360MM / STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDS·November 28, 2023

    LOCKING SCREW FOR IM NAIL Ø 5MM/ 86MM/ XL25/ STERILE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·September 11, 2023

    CRANIAL-SCR PLUSDRIVE Ø1.6 SELF-DRILL L4

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 23, 2023

    MEDIAL ROTATION KNEE® LEFT TIBIAL INSERT SIZE 2, 10.5MM

    FDA Adverse Event
    Malfunction ·FINSBURY ORTHOPAEDICS LIMITED·Product code JWH·June 19, 2023

    TI LOW PROFILE NEURO SCREW SELF-DRILLING 4MM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JEY·April 7, 2023