BEUDAMED
    13 results · 43ms · Sources: EU EUDAMED, US FDA

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    US MEDCO, INC.

    FDA registration
    US MEDCO, INC.·5 products·🇺🇸 United States

    USMEDCO

    FDA UDI
    US MEDCO INC·08600036785340·SPONGE LAP WASHED 18" x18"

    USMEDCO

    FDA UDI
    US MEDCO INC·08600036785272·SPONGE LAP WASHED 18" x18"

    USMEDCO

    FDA UDI
    US MEDCO INC·08600036785418·SPONGE LAP WASHED 12" X 12"

    USMEDCO

    FDA UDI
    US MEDCO INC·08600036785586·SPONGE LAP WASHED 12" X 12"

    USMEDCO

    FDA UDI
    US MEDCO INC·08600036785654·SPONGE LAP WASHED NO LOOP

    US MEDCO INC.

    FDA Adverse Event
    Malfunction ·US MEDCO INC.·Product code GDY·December 12, 2018

    OR TOWEL, BLUE, X-RAY DETECT., GEOMED, STERILE, 4/PK, 20PK/CS

    FDA Adverse Event
    Malfunction ·US MEDCO INC.·Product code FRL·August 7, 2024

    US MEDCO INC

    FDA Adverse Event
    Malfunction ·US MEDCO, INC.·Product code GDY·June 1, 2018

    18 X 18 X R 5S NO RING

    FDA Adverse Event
    Injury ·US MEDCO, INC.·Product code GDY·September 30, 2016

    OR SAFETY TOWEL

    FDA Adverse Event
    Malfunction ·US MEDCO, INC.·Product code FRL·May 12, 2016

    TOTAL KNEE PACK A & B

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code LRO·November 26, 2019

    XEN Gel Stent, REF 5513-001(US Model), Sterile, RX Only, (01)10888628032439 ; Other Model Numbers: 5507-001(Global Model) and 5517-001(Australia model) Implant for glaucoma treatment.

    FDA Recall
    Open, Classified ·Allergan PLC·Product code KYF·October 30, 2019