BEUDAMED
    23 results · 28ms · Sources: EU EUDAMED, US FDA

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    Transcutaneous Electronic Nerve Stimulator

    FDA 510(k)
    FDA Class 2 ·Neurology

    MICRO TYING FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896060630·MICRO TYING FORCEPS CURVED TUNGSTEN CARBIDE DUS...

    PROFYLE

    FDA UDI
    Stryker GmbH·04546540256034·Drill Guide, M, Eccentric

    Accent Buccal Tube

    FDA UDI
    ORMCO CORPORATION·00889989054279·ORTHOS ACCENT ODBL LFM -10X22X21 RT

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780182344·Integra® Jarit® Willauer-Deaver Retractor, 15",...

    Sonoma™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981050832·Sonoma Anterior Cervical Plate 2 Level Plate, 37mm

    Manta Ray™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981057107·Plate - 2 Level - 37 mm

    EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMMUNOASSAY PLUS CONTROL, LEVELS 1, 2, AND 3

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 23, 2022

    T:SLIM X2 INSULIN PUMP

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code LZG·March 12, 2019

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 30, 2023

    T:SLIM G4 SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code OYC·June 14, 2019

    T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY (WITH T:CONNECT MOBILE APP)

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·May 21, 2024

    FUSION QUATTRO EXTRACTION BALLOON

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code GCA·December 10, 2024

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·August 11, 2011

    CLOSUREFAST CATHETER, 7F, 100CM

    FDA Adverse Event
    Injury ·COVIDIEN-PLYMOUTH·Product code GEI·October 24, 2014

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 1, 2013

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·April 10, 2017

    FUSION QUATTRO EXTRACTION BALLOON

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code GCA·June 7, 2024