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

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    CEREGLIDE 71 Intermediate Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Pinnacle®

    FDA UDI
    Ortho Organizers, Inc.·00190707111892·Pinnacle .022 MC UR 4/5 HK G/O -7T 0A 0O (10PK)

    Votion

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730008077·Votion .022 MC UR 4/5 HK G/O -7T 0A 0O (10PK)

    Votion®

    FDA UDI
    Ortho Organizers, Inc.·00190707113766·Votion .022 MC UR 4/5 HK G/O -7T 0A 0O (10PK)

    Pinnacle

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730009906·Pinnacle .022 MC UR 4/5 HK G/O -7T 0A 0O (10PK)

    MEDICA EASYQC BLOOD GAS/ELECTROLYTE CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Nanum Syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BIO-MODULAR HUMERAL HEAD EXTENDED ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWT·March 29, 2017

    PLUS SL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPEDICS AG·Product code KWY·November 5, 2008

    MAXPLUS BI-FUSE EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·August 17, 2011

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·July 5, 2013