BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    SYSTEM 2 ZIPPERED BODY HOLDER, SMALL/MEDIUM 24453-010,24453-020,24453-030

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PEAK BOND, MODEL 5133

    FDA 510(k)
    FDA Class 2 ·Dental

    SS SA Fixture

    FDA 510(k)
    FDA Class 2 ·Dental

    21 REC CANISTER

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD·Product code GCX·April 10, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FPO·February 1, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·December 20, 2010

    PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 15, 2025

    GII OVAL RESURFACING PAT 32MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·December 18, 2015

    CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026