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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ScalpelCric

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ISOLA

    FDA UDI
    DEPUY SPINE, LLC·10705034006444·ISOLA SPINE SYSTEM OPEN HOOK 4.75 x 5.0mm

    MICRO FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896060425·MICRO FORCEPS WITH PLATFORM STRAIGHT TUNGSTEN C...

    KNOWLES BANDAGE SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896054424·KNOWLES BANDAGE SCISSORS ANGLED BLADE POWER CUT...

    BIO-DETEK ELECTRODE ADAPTER, MODEL R2001-90

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    PORTADUR P 4

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO CARTO EP NAVIGATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·August 11, 2011

    UNICEL DXI 800 ACCESS IMMNOASSAY SYSTEM

    FDA Adverse Event
    Other ·BECKMAN COULTER, INC.·Product code MMI·September 24, 2008

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 1, 2013

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 21, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 25, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 15, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 20, 2021