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

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    CRANE ACRYLIC HERBST APPLIANCE

    FDA 510(k)
    FDA Class 2 ·Dental

    AGXO

    FDA UDI
    Oticon A/S·05707131270184·H110, DESIGNRITE 10 WL SGR AGXO

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197382939·Mixter Kidney Pedicle Clamps curved...

    PROSIM 4, PROSIM 6, PROSIM 8

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    URGOCELL AG, ANTIMICROBIAL WOUND DRESSING WITH SILVER

    FDA 510(k)
    FDA Unclassified ·Unknown

    PRESIDIO 10 CERE 5MMX17CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code HCG·December 28, 2021

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 31, 2013

    WIRE COLLET

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENT KALAMAZOO·Product code GET·June 17, 2011

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code KRG·October 3, 2014

    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