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

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    USTOMED Bone Fixation/Bone Augmentation Systems - PIN

    FDA 510(k)
    FDA Class 2 ·Dental

    Syntec-Taichung Non-sterile Bone Plate and Screw Implants

    FDA UDI
    SYNTEC SCIENTIFIC CORPORATION·04719864684955·Straight Mini Plate 2.0 x 20Holes x L100mm

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114148·SIMCOE I/A SYSTEM 23GA (PK/3)

    JOURNEY TIBIA BASE NP RT SZ 3

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·April 16, 2019

    TAPERLOC COMPLETE RASP/PROVISIONAL

    FDA UDI
    Biomet Orthopedics, LLC·00880304632530·

    SCALLOPED ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Eye Secret 38 UV Aspheric (polymacon) 1-Day Soft (hydrophilic) Contact Lens

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ARTICUL/EZE BALL 32 +1 GR

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD.·Product code JDI·November 11, 2014

    UNKNOWN DEPUY ASR HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·September 12, 2011

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 23, 2013

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 16, 2018