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

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    Arthrex MaxForce MTP Compression Plates and Screws

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777679·LUMBAMED BASIC DORSAL STAYS M SILVER V

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·04049958003868·600 micron Holmium Laser Fiber Cable, Reusable,...

    Fluid Retention Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112854·VIDAURRI FLUID RETENTION WELL 8.7MM

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613153153771·Z-PLATTE RIGHT, BAR LENGTH 12MM

    Ballard* Closed Suction System for Adults

    FDA UDI
    Avanos Medical, Inc.·00609038987835·BALLARD* Closed Suction Catheter, T-Piece

    CRANIAL LOOP CRANIAL BONE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    OPTI-FREE SUPRACLENS DAILY POTEIN REMOVER / RGP MULTI-PURPOSE DISINFECTING SOLUTION ID 100136

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    2520274-2013-05122

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 27, 2013

    2520274-2013-05114

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 27, 2013

    2520274-2013-05116

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 27, 2013

    2520274-2013-05093

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 27, 2013

    2520274-2013-05102

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 27, 2013

    2520274-2013-05145

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 26, 2013

    2520274-2013-05117

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 27, 2013

    2520274-2013-05112

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 27, 2013

    2520274-2013-05148

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 26, 2013

    2520274-2013-05064

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 27, 2013

    2520274-2013-05069

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 26, 2013

    2520274-2013-05118

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 27, 2013