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

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    LC SPRINT NEBULIZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DIATEK CANNON-CATH #CC2400, CC2800, CC3200, CC3600,CC5500. CC2400PC, CC2800PC, CC3200PC(32 CM), CC3200PC(36 CM)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    STC PCP INTERCEPT MICRO-PLATE EIA, MODEL 11541

    FDA 510(k)
    FDA Unclassified ·Unknown

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 10, 2013

    SUMMIT POR TAPER SZ5 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 4, 2014

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code MMI·April 15, 2011

    UNK KNEE PATELLA SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·July 6, 2022

    UNK KNEE TIBIAL TRAY SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·July 6, 2022

    UNK KNEE FEMORAL SIGMA PS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·July 6, 2022

    UNK KNEE TIBIAL INSERT SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·July 6, 2022

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018