BEUDAMED
    133 results · 22ms · Sources: EU EUDAMED, US FDA

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    Optilite CH50 Reagent, Optilite CH50 Controls and Optilite CH50 Calibrator

    FDA 510(k)
    FDA Class 2 ·Immunology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526768468·GENUMEDI PSS GREEN II

    AGXO

    FDA UDI
    Oticon A/S·05707131288554·H110V2, DESIGNRITE 10 WL CBE AGXO

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00880304006485·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100066·TEMPORAL SPECULUM CLOSED WIRE

    MORRISON MEDICAL

    FDA UDI
    MORRISON MEDICAL, LTD·00647921150416·CTR FOAM CDBD SPLINT 12" CS 12

    Admiral

    FDA UDI
    Seaspine Orthopedics Corporation·10889981277338·Trial Drill Guide, 15/15 Deg, 12mm

    Femoral Sizer ML Check 5

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215074487·

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962104729·ROUND BURR, 5.5MM, S

    Non-Shouldered Restorative Kit

    FDA UDI
    BICON, LLC·00813110024985·5.0 x 12mm Non-Shouldered Restorative Kit

    Sklar

    FDA UDI
    SKLAR CORPORATION·30649111324141·REUSBLE SOLUTION BOWL 7QT PK12

    UNKNOWN OSS TIBIAL BUSHING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 20, 2019

    UNKNOWN OSS LOCKING PIN

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 20, 2019

    OSS TIBIAL POLY BEARING

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·December 4, 2018

    BIOLOX DELTA CERAMIC FEMORAL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VAPORMAX

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

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962102732·DISPOSABLE ARTHROSCOPIC 5.5mm ROUND BURR, COMPA...

    OSS REINFORCED YOKE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·May 9, 2023

    MBT CEM KEEL TIB TRAY SZ4

    FDA Adverse Event
    Injury ·9616671 DEPUY IRELAND·Product code NJL·June 6, 2013

    ECHELON 60

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 6, 2011