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

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    3MTM AttestTM Mini Auto-reader 490M

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Vivos mmRNA

    FDA UDI
    FIVE STAR ORTHODONTIC LABORATORY & SUPPLY INC·D82852000920·

    Darby Dental Supply, LLC

    FDA UDI
    DARBY DENTAL SUPPLY, LLC·00889813028292·MOUTH PROP BLACK NON-LATEX M DARBY

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·00304040187937·ZIRLUX ML DISC C4 98x22

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694006118·1.3mm Pilot Drill, 3.5mm Stop, Manual

    DEBAKEY NEEDLE PULLING FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896059627·DEBAKEY NEEDLE PULLING TISSUE FORCEPS TUNGSTEN ...

    Locking Cannulated Blade Plate

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132134627·BMP GUIDE (3.2MM DRILL BIT)

    TEMPHASE

    FDA 510(k)
    FDA Class 2 ·Dental

    CORVUS RADIATION THERAPY PLANNING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    RESOLUTION CLIP DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MND·October 15, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011

    TI NUT 11MM WIDTH ACROSS FLATS

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·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