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

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    WU'S 3-WHEELED NEO SCOOTER, WT-T3B

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114001·CHANG HYDRO-DISSECT CANNULA 27GA

    CONMED

    FDA UDI
    Conmed Corporation·10845854006023·MICRO OSCILLATOR BLADE, FINE, 10 X 13 X 0.4 MM 20°

    IMUBIND PLASMA PAI-1 ELISA,MODEL 822

    FDA 510(k)
    FDA Class 2 ·Hematology

    MICROSCAN SYNERGIS PLUS GRAM NEGATIVE MIC/COMBO PANELS WITH TOBRAMYCIN (0.12-32 UG/ML)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SEE H10

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KXA·November 1, 2011

    INNOVA 4100

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS·Product code MQB·April 4, 2011

    INNOVA 4100

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS·Product code MQB·May 6, 2011

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF0231689040338217201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF023168904033217201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF023168904031217201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF0231689040315917201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF023168904031317201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF0231689040312717201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF0231689040338117201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF023168904032517201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF0231689040312017201·BTE-TRT

    FEMORAL HEAD PROVISIONAL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code FZX·October 21, 2020

    Hydrodissection Cannula (Chang), 27g, labeled as: anodynesurgical, REF 7018 ASICO, REF AS-7638 anodynesurgical, REF 7018NS katena, REF K20-3168 anodynesurgical, REF 104910 MSI, REF CA7800 ACCUTONE, REF AX14784-BULK Walcott Rx Products, REF RX2300NS Walcott Rx Products, REF RX2300

    FDA Enforcement
    Class II ·Terminated·Anodyne Surgical·June 23, 2021

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCO·Product code CBK·February 27, 2013