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

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    LymphaTech Mobile 3D Measuring Tool

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    EasyTouch

    FDA UDI
    MHC MEDICAL PRODUCTS, LLC·MHC182512552·ET 25G 1" 1mL Syringe w/ exchangeable needle (TB)

    ceraMotion®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011251255200·ceraMotion® Ti Touch Up Dentin light, 20 g / de...

    Navigator Aesthetic Delivery System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LUMIPHASE-R

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

    Vu aPod™ - L

    FDA UDI
    Seaspine Orthopedics Corporation·10889981046927·LATERAL TRIAL, WIDE, LORDOTIC, 12mm X 23mm X 55...

    NA

    FDA UDI
    aap Implantate AG·04042409261466·Cortical Screw 2.5, small head T8, self-tapp. L 55

    SINGLE 8 EXTENSION, 60 CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·September 12, 2011

    NATRELLE SILICONE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGEN, INC·Product code FTR·November 5, 2014

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 29, 2013

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·April 3, 2024

    UNK HIP ACETABULAR LINER POLY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·April 26, 2024

    UNK HIP FEMORAL HEAD METAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·April 26, 2024

    UNK HIP FEMORAL STEM CHARNLEY

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code LPH·April 26, 2024

    Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: FlexViewing PC Azurion Model Name - Model Number: Azurion 7 B12 722067; Azurion 7 B20 722068; Azurion 7 M12 722078 722223; Azurion 7 M20 722079;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 28, 2024

    Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: XRay PC, Suite PC, and FlexViewing PC Azurion Model Name - Model Number: Azurion 3 M12 722063 722221; Azurion 3 M15 722064 722222; Azurion 5 M20 722228; Azurion 7 B12 722067 722225; Azurion 7 B20 722068 722226; Azurion 7 M12 722078 722223; Azurion 7 M20 722079 722224;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 28, 2024

    Allura Xper FD20 Product Codes: (1)722012, (2) 722028, (3) 722006; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·October 1, 2025

    ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026

    Allura Xper FD10; Model Numbers: (1) 722003, (2) 722010, (3) 722026; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·October 8, 2025