BEUDAMED
    26 results · 25ms · 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 ×

    TrueView Core 100Pro-US Core Specimen Radiography System (TrueView Core 100Pro-US)

    FDA 510(k)
    FDA Class 2 ·Radiology

    NuVasive

    FDA UDI
    Nuvasive, Inc.·00887517193629·Universal Holder, Initial Dilator

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361036135·SCREW, SOLID WALL, CANNULATED, Ø10MM X 40MM, SA...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197306942·Hartmann aural tampon forceps 4 3/4"...

    INTRA-LOCK OP DENTAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Dental

    DUOMED, SERIES 500, (MODELS ID 500, FL 500)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Quantum

    FDA UDI
    QUANTUM BIOENGINEERING LTD.·D825230140011HA0·Thread Implant 3W 4.0 X 11 HA

    Quantum

    FDA UDI
    QUANTUM BIOENGINEERING LTD.·D825230140009HA0·Thread Implant 3W 4.0 X 9 HA

    Quantum

    FDA UDI
    QUANTUM BIOENGINEERING LTD.·D825230140014HA0·Thread Implant 3W 4.0 X 14 HA

    Quantum

    FDA UDI
    QUANTUM BIOENGINEERING LTD.·D825230140008HA0·Thread Implant 3W 4.0 X 8 HA

    Quantum

    FDA UDI
    QUANTUM BIOENGINEERING LTD.·D825230140005HA0·Thread Implant 3W 4.0 X 5 HA

    Quantum

    FDA UDI
    QUANTUM BIOENGINEERING LTD.·D825230140006HA0·Thread Implant 3W 4.0 X 6 HA

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 21, 2020

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code MGB·November 25, 2015

    M2A MAGNUM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·December 26, 2025

    COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·November 17, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 1, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    TAIWAN ANI CO., LTD.·Product code IOR·July 16, 2013

    SELEX / M2A-MAGNUM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·December 26, 2025

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 6, 2016