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

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    Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    Richard Wolf GmbH·04055207012017·CO2 CONNECTING TUBE

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111013553·SKLARLITE ALLIS FCP 5X6 6

    BD VACUTAINER® 9NC 0.129M PLUS BLOOD COLLECTION TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 22, 2021

    MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PEEK CAGE FOR THE VERTEBRAL SPINE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·November 18, 2008

    ASR ACETABULAR IMPLANT 60

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 18, 2011

    2520274-2013-04482

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 18, 2013

    Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);

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