BEUDAMED
    19 results · 35ms · Sources: EU EUDAMED, US FDA

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    PERFRACTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    SimPro™ Now

    FDA UDI
    Wellspect AB·07392532188299·Single Use Urinary Catheter with water sachet. ...

    COLIBRI TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896073364·COLIBRI TISSUE FORCEPS DELICATE TIPS TITANIUM

    COLIBRI FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896015357·COLIBRI TISSUE FORCEPS DELICATE TIP STAINLESS S...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702435559·Elvarex Forte 3/Thigh High/Slant-Open Toe-Eleph...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702472776·E3/AG/OT-E/NOP5-T-OH/BLU

    SureCore Semi-automatic Disposable Biopsy Needle

    FDA UDI
    Canyon Medical Inc.·06954414659337·Semi-automatic Disposable Biopsy Needle

    SureCore Semi-automatic Disposable Biopsy Needle

    FDA UDI
    Canyon Medical Inc.·06954414659412·Semi-automatic Disposable Biopsy Needle

    SureCore Semi-automatic Disposable Biopsy Needle

    FDA UDI
    Canyon Medical Inc.·06954414659498·Semi-automatic Disposable Biopsy Needle

    POINT 500 HD POINT500C HD

    FDA 510(k)
    FDA Class 2 ·Dental

    SENSITITRE SUSCEPTIBILITY PLATES

    FDA 510(k)
    FDA Class 2 ·Microbiology

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 14, 2024

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 27, 2011

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025