BEUDAMED
    23 results · 31ms · Sources: EU EUDAMED, US FDA

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    Apollo Ankle Fracture Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    n.a.

    FDA UDI
    Karl Storz GmbH & Co. KG·04048551072820·FISCH Dura Elevator, length 16 cm

    RIGIDFIX

    FDA UDI
    Medos International Sàrl·10886705019960·RIGIDFIX CURVE Arc Attachment Arc Attachment

    Tick Removal Kit - zlb

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588160054·Tick Removal Kit - zlb

    Micro Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR77812130051·Micro Sprint Bracket McLaugh/Benn/Trev. .018" m...

    Mini-Mono®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR77522130051·High-Tech-Brackets Alexander 'S' .018" f. weld....

    DDRVERSA MOTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACT 11 MP VENTRICULAR CATHETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    FG 6301 DUAL CHNL VOL INF PUMP

    FDA Adverse Event
    BAXTER HEALTHCARE (SG)·Product code FRN·October 29, 2008

    RENAISSANCE 29

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·July 12, 2011

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI PLANT - ST. PAUL·Product code NVY·July 9, 2013

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·February 20, 2026

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·January 23, 2026

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·June 25, 2025

    MAZOR X SYSTEM

    FDA Adverse Event
    Malfunction ·MAZOR ROBOTICS LTD·Product code OLO·January 1, 2026

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·January 23, 2026

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·January 29, 2026

    MAGNETOM Cima.X (DE). Model Number: 11647158.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025