BEUDAMED
    26 results · 21ms · Sources: EU EUDAMED, US FDA

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    SYNGO CT PULMO 3D

    FDA 510(k)
    FDA Class 2 ·Radiology

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169606623·SPACER 2123540 O25 23.5MM 18 DEG 16X40

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517421180·CoRoent LO Trial, 12x10x35/40 5°

    Respiratory Suppr. Plate, L

    FDA UDI
    MACROMEDICS B.V.·08719425702636·Respiratory Suppression Plate for SBRT Secure A...

    NorthStar

    FDA UDI
    Seaspine Orthopedics Corporation·10889981231729·W Parallel Top Loading

    Atoll™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981052447·3.5mm x 40mm Poly Screw Assm. The Atoll OCT Spi...

    GLOBAL CAP CTA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295018018·GLOBAL CAP CTA HEAD DUOFIX HA SIZE 40 x 15 CEME...

    Sochi

    FDA UDI
    Altus Spine, LLC·00843210166551·Polyaxial Screw, 3.5mm x 40mm

    GLOBAL CAP CTA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295018025·GLOBAL CAP CTA HEAD DUOFIX HA SIZE 40 x 18 CEME...

    PSORIA-LIGHT

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

    SNAP KOVER, MODEL 01-2020; SNAP KAPS, MODEL 03-KP09

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

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    ARTICUL/EZE BALL 28 +12 BLK

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JDI·May 22, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 26, 2014

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·June 9, 2011

    ILIAC SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019

    POLARIS SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020

    MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.

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

    TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 15, 2017