BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    Portrait VSM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GOMCO

    FDA UDI
    Allied Medical, LLC·00026072001936·ASPIRATOR, SURGICAL 220V/50HZ

    VC150 VITAL SIGNS MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·November 6, 2014

    CHISEL BLADE W/16

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZO·July 18, 2013

    GYNECARE TVT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·November 18, 2015

    M2A-MAGNUM PF CUP 54ODX48ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 5, 2018

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·January 23, 2026

    TIGHTRAIL ROTATING DILATOR SHEATH

    FDA Adverse Event
    Death ·SPECTRANETICS CORPORATION·Product code DRE·May 22, 2026

    GLIDELIGHT LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORPORATION·Product code MFA·May 22, 2026

    GLIDELIGHT LASER SHEATH

    FDA Adverse Event
    Death ·SPECTRANETICS CORPORATION·Product code MFA·May 22, 2026

    TIGHTRAIL ROTATING DILATOR SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORPORATION·Product code DRE·May 22, 2026