BEUDAMED
    16 results · 29ms · Sources: EU EUDAMED, US FDA

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    PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA.

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

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556708276·GC Initial™ Zr-FS Frame Modifier FM-5, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228750051·GC Initial™ Zr-FS Frame Modifier FM-5, 20g

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668109496·BISHOP-HARMON SILICONE BULB AND ADAPTOR

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867263703·PRFL DRL, 5.0MM CMPR FT

    Arthrex

    FDA UDI
    Provision·B504OMAR8750050·

    FIBER MESH

    FDA 510(k)
    FDA Class 2 ·Dental

    BROOKER ACETABULAR CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867319578·PRFL DRL, 5.0MM LG CMPR FT SCRW, REUSE

    PRFL DRL, 5.0MM CMPR FT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HTW·August 11, 2023

    V.A.C. ATS

    FDA Adverse Event
    Injury ·KCI USA, INC.·Product code OMP·June 2, 2014

    SM104 MSERIES W5TH WHL

    FDA Adverse Event
    Malfunction ·STRYKER CORP. MEDICAL DIVISION·Product code FPO·October 13, 2010

    LIGACLIP

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code FZP·December 13, 2012

    UNIVERSAL IMPACTOR/POSTIONER

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·October 10, 2017

    G-WIRE W/TRCR TIP, THDD, 062"X9.25"

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code LXH·March 9, 2020

    COMPR FT SCRW, 5.0 LG, 40MM LGTH

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 9, 2020