BEUDAMED
    15 results · 21ms · Sources: EU EUDAMED, US FDA

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    CATHETER CONNECTOR, ARGYLE TUBING

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Ortho Specialties

    FDA UDI
    Young Innovations, Inc.·00840326414088·Bicuspid Bands, Upper, Size 24

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110652·COAXIAL IRR-ASP TIP 45 DEG W/ SILICONE

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110669·COAXIAL IRR-ASP- TIP 90 DEG- W/ SILICONE

    NRFit

    FDA UDI
    ICU MEDICAL, INC.·10610586044113·

    FibroScan 530 Compact

    FDA 510(k)
    FDA Class 2 ·Radiology

    DOLPHIN 2000 DATEX COMPATIBLE OXIMETRY DISPOSABLE AND REUSABLE SENSORS AND EXTENSION CABLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CADD EXTENSION SET

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·July 6, 2020

    NRFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·July 2, 2024

    CADD

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·July 13, 2021

    NRFIT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·September 25, 2020

    M2A-MAGNUM 42-50MM TAPER INSERT-6

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·April 21, 2014

    GYNECARE MORCELLEX* TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·September 26, 2012

    SIG MOD TIB TRAY CEM COCR 2

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 15, 2010

    Heritage Labs Appraise A1c Diabetes Home Test , Product K7609, 24 kits/shipping carton (Product K7609), each kit packed in a box and contains 1 Triad Medium Alcohol Prep Pad, Cat. No. 10-3001, NDC 50730-3001-0, and blood specimen collection supplies, forms, and instructions Blood specimen collection

    FDA Recall
    Terminated ·Heritage Labs International LLC·Product code LCP·January 9, 2011