BEUDAMED
    4,653 results · 28ms · Sources: EU EUDAMED, US FDA

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    ACUMED ANATOMIC RADIAL HEAD SYSTEM, ACUMED ANATOMIC RADIAL HEAD LONG STEMS, ACUMED ARH SLIDE-LOC

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741318450·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674131845060·

    Oticon

    FDA UDI
    Oticon A/S·05707131259196·NERA PRO, KIT 13 DIR R H BE

    Precise

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657008105·Maryland Jaw, 5mm, 45cm, Standard Handle

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587C13184540·13mm H x 18mm W x 45mm L x 4 degree XLIF Corona...

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102244·SLOANE LASEK EPI PEELER

    Precise

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657075435·Precise Maryland Jaw, 5mm, 45cm Insert

    Precise

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657008112·Precise Maryland Jaw with Ratchet,

    Precise

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657068888·Precise Maryland Jaw, 5mm, 45cm Insert

    Precise

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657086059·Precise Maryland Jaw, 5mm, 45cm, Standard Handl...

    Freedom Pedicle Screw System

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215027254·

    THE ESPINER SAC OR E SAC

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TUBING, CONMNECTORS, AND ACCESSORIES WIT BALANCE BIOSURFACE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    5.0MM LOCKING SCREW SLF-TPNG WITH T25 STARDRIVE RECESS 40MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KTT·May 29, 2013

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 20, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 14, 2022