BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ARx Modular Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HHM

    FDA UDI
    Sbo Hearing A/S·05714464006526·F50 FW 1.0.0

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180136175·ELMED LAPAROSCOPIC TROCAR INCISION WOUND CLOSUR...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776199524·LAPAROSCOPIC INCISION CLOSURE DEVICE

    PLASTIC NEEDLE WITH MANDRIN 2.0 DIAMETER LENGTH 113MM

    FDA 510(k)
    FDA Class 2 ·Radiology

    GIVEN DIAGNOSTIC SYSTEM

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

    SMR SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·May 11, 2026

    BARRIGEL INJECTABLE GEL

    FDA Adverse Event
    Malfunction ·PALETTE LIFE SCIENCES·Product code OVB·June 24, 2024

    PFC MOD C/S STAB INS SZ5 10MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·November 3, 2008

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·August 23, 2011

    FORTIFY DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 11, 2013