BEUDAMED
    22 results · 33ms · Sources: EU EUDAMED, US FDA

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    EEA Circular Stapler with Tri-Staple Technology

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111062·INSTRUMENT CASE MEDIUM ALUMINUM

    PIN SCREW

    FDA UDI
    BK MEDITECH CO.,LTD.·08809155854948·Wire Pin Screw, 2.3mm Shaft Diameter x 2.3mm Th...

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819233000101·EXMRC ROTH 022/LL3 - 11T 7A 2M

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819233000201·EXMRC MBT 022/LL3 - 6T 3A

    OC-SENSOR DIANA IFOB TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTELLAMAP ORION?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·May 12, 2026

    INTELLAMAP ORION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 15, 2025

    INTELLAMAP ORION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 29, 2026

    INTELLAMAP ORION?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 17, 2026

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 18, 2013

    ISOFLEX LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DTB·January 11, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011

    INTELLAMAP ORION?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·January 30, 2026

    INTELLAMAP ORION?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 1, 2026

    INTELLAMAP ORION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·November 21, 2024

    INTELLAMAP ORION?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·February 26, 2026

    M2A-MAGNUM MOD HD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 5, 2018

    M2A-MAGNUM PF CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 5, 2018