BEUDAMED
    18 results · 23ms · Sources: EU EUDAMED, US FDA

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    e-motion M25

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TLS 5.0

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030CK2212150·Enhanced Graft Interbody Cage 7DEG x 22L x 12W ...

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981215491·No-Profile Interbody, 39mm x 27mm x 12mm, 15 Deg

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365118449·

    Foundation Surgical Interwedge

    FDA UDI
    FOUNDATION SURGICAL GROUP INC·00810141040335·Trial - 22x12x15

    Symmetry Surgical®

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482044803·Symmetry® Retractor, Collins, Double-Ended, 6 1...

    SenoBright HD

    FDA 510(k)
    FDA Class 2 ·Radiology

    BIO-LOGIC ABAER CUB

    FDA 510(k)
    FDA Class 2 ·Neurology

    HNM Medical

    FDA UDI
    HNM STAINLESS, LLC.·00842962113745·COLLINS RETRACTOR, 6 1/2", DOUBLE ENDED, SET OF 2

    SMR SHOULDER

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·July 25, 2025

    CAPTURE-R READY-SCREEN 3

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code QHT·March 21, 2023

    ENCORE

    FDA Adverse Event
    Injury ·ARJO MED AB LTD.·Product code FSA·November 5, 2008

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 24, 2011

    KINETIX?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·July 11, 2013

    BD ALLERGY SYRINGE TRAY WITH BD SAFETYGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code MEG·May 3, 2023

    SOL-MILLENNIUM

    FDA Adverse Event
    Malfunction ·SOL-MILLENNIUM MEDICAL INC·Product code GAA·May 16, 2025

    BIOMET StageOne Hip Cement Spacer Mold with Insert, 56 MM, Silicone, Sterile, Item 431183.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020

    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V

    FDA Enforcement
    Class II ·Terminated·Roche Diagnostics Corporation·March 14, 2018