BEUDAMED
    26 results · 24ms · Sources: EU EUDAMED, US FDA

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    LINK® MEGASYSTEM-C®

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AGXO

    FDA UDI
    Oticon A/S·05707131282675·H110V2, BTE 13 WL 85 SIL AGXO

    AGC Tradition Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304001763·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100028·BLUMENTHAL SPECULUM X-HEAVY

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180162020·BURR (22M)

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613043827·Brown AutoClavable Surgical Identification Tape...

    Symmetry Hudson

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482000342·Symmetry® Burr; Hudson; 22 mm

    VARIANT

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPO1510080·Threaded Fixation Pin, 80mm

    NA

    FDA UDI
    aap Implantate AG·04042409192289·Cortical Screw 1.5, self-tapping, L 8

    DIGITAL COLOR DOPPLER ULTRASOUND IMAGING SYSTEM, CONVEX ARRAY TRANSDUCER, LINEAR ARRAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    SET

    FDA 510(k)
    FDA Class 2 ·Dental

    NA

    FDA UDI
    aap Implantate AG·04042409192432·Cortical Screw 1.5, self-tapping, L 8

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    CONSMA·Product code ITJ·June 6, 2013

    AUGMENTED INSERT

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·June 30, 2011

    GEMSTAR PUMP SET WITH 0.2MICRON FILTER AND PA-ASV

    FDA Adverse Event
    Malfunction ·HOSPIRA DE COSTA RICA LTD.·Product code FRN·August 28, 2008

    MICROVASCULAR PLUG

    FDA Adverse Event
    Injury ·REVERSE MEDICAL·Product code KRD·September 8, 2021

    MICROVASCULAR PLUG

    FDA Adverse Event
    Injury ·REVERSE MEDICAL·Product code KRD·September 8, 2021

    LIFE SCOPE G9

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·June 13, 2024

    LIFE SCOPE G9

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·October 27, 2023

    BELLAFILL DERMAL FILLER

    FDA Adverse Event
    Injury ·SUNEVA MEDICAL, INC.·Product code LMH·October 13, 2022