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

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    MIRADA RTX

    FDA 510(k)
    FDA Class 2 ·Radiology

    ArgenZ HT+ 98x25 ML B1B

    FDA UDI
    ARGEN CORPORATION, THE·D818130393·Dental porcelain/ceramic restoration kit

    EVONOS GMBH & Co. Kg

    FDA UDI
    Gyrus ACMI, LLC·00821925011991·JORDAN CAPSULE KNIFE 1 MM BLADE LENGTH STAINLES...

    LCU Hip System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575415618·Orthopaedic implant aiming/guiding block, reusa...

    Lubinus Classic Plus Hip Stem - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575286263·Surgical instrument handle, non-torque-limiting...

    Direct Anterior Approach - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575192830·Surgical instrument handle, non-torque-limiting...

    LINK Instruments - Handles and adapters

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575411375·Surgical instrument handle, non-torque-limiting...

    Direct Anterior Approach - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575192816·Surgical instrument handle, non-torque-limiting...

    POLARIS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTICAL LOW COHERENCE REFLECTOMETRY (OLCR) PACHYMETER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LIT·August 24, 2017

    ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LIT·August 24, 2017

    WAVEWRITER ALPHA? 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 30, 2025

    CONSERVE(R) FEMORAL HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·May 24, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011

    HUT EXT DR FINAL ASSY-REVERSE

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code KQS·August 20, 2008

    ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LIT·May 31, 2017

    ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LIT·March 30, 2017

    ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LIT·July 27, 2017

    ADVANCE 18 LP LOW PROFILE PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LIT·November 16, 2016